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CC Cream Broad Spectrum SPF 30 Merle Norman Homosalate, Octinoxate, Oxybenzone, Titanium Dioxide 7 g/100g; 2.5 g/100g; 2 g/100g; 4.1 g/100g Cream

by Merle Norman Cosmetics, Inc · 1 TUBE in 1 CARTON (57627-170-02) / 35 g in 1 TUBE (57627-170-01)
NDC 57627-0170-02
🏷️ FDA NDC (as labeled) 57627-170-02 billing pads the product segment with a zero
OTC On market Non-controlled
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

🆔 Identity & classification

FDA NDC (as labeled) 57627-170-02
Product NDC 57627-170
11-digit billing NDC 57627017002
UNII V06SV4M95S, 4Y5P7MUD51, 95OOS7VE0Y, 15FIX9V2JP
Application # M020
SPL Set ID 93ebe819-6763-400c-8320-812276168b6c
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2014-06-19
Route TOPICAL
Dosage form CREAM
Substance HOMOSALATE; OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE
Why two NDCs? The FDA registers this code as 57627-170-02 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 57627-0170-02. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

🏭 Manufacturer & labeler

LabelerMerle Norman Cosmetics, Inc
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code57627
First marketedJun 2014
Product typeHuman Otc Drug
Portfolio48 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

🩺 Clinical

🧪 What is this product?

This is a topical cream marketed as a color-correcting cosmetic with broad spectrum sun protection. It contains four active ingredients that function as ultraviolet (UV) filters: homosalate, octinoxate, and oxybenzone are chemical UV absorbers, while titanium dioxide is a mineral UV reflectant. Together these ingredients are typically used to help protect skin from UVA and UVB sun damage. This product is an over-the-counter monograph drug, meaning it is marketed under the FDA's established rules for sunscreen products rather than as an individually approved application.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

🧪 Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII 9E8X80D2L0
    A synthetic form of vitamin E used as an antioxidant and preservative in medications. It helps prevent the active ingredients from degrading when exposed to oxygen or light.
  • UNII A9EJ3J61HQ
    A synthetic liquid derived from benzoic acid and long-chain alcohols. It functions as a solvent and penetration enhancer in topical formulations, helping active ingredients dissolve and absorb into the skin.
  • UNII KZJ3T010RQ
    A chemical compound containing aluminum and hydrogen. It may serve as a reducing agent or reactant in pharmaceutical manufacturing to help produce or stabilize active ingredients during drug formulation.
  • UNII B423VGH5S9
    A natural fruit ingredient derived from apples, used as a flavoring agent and sweetener to improve taste and palatability of the medicine.
  • UNII 3XUS85K0RA
    Butylene glycol is a clear liquid derived from petroleum or plants that acts as a humectant, solvent, and preservative booster in medicines. It helps keep formulations stable, dissolve active ingredients, and maintain moisture in topical products.
  • UNII 00YIU5438U
    Caprylyl glycol is a clear liquid derived from coconut oil. In medicines, it acts as a humectant to retain moisture, a preservative booster to prevent microbial growth, and a solvent to help dissolve or mix other ingredients.
  • UNII V2W71V8T0X
    A silicone-based compound that mixes oil and water together. Used in formulations as an emulsifier to help blend ingredients and improve texture and stability of creams, lotions, and other topical products.
  • UNII 0THT5PCI0R
    A silicone-based liquid that helps distribute active ingredients evenly throughout topical products. It acts as a solvent and emollient, allowing medicines to spread smoothly on skin while improving texture and absorption.
  • UNII 92RU3N3Y1O
    Dimethicone is a silicone-based oil that acts as an anti-foaming agent and lubricant in medicines. It reduces gas bubbles in liquid formulations and helps coat and protect the stomach lining when ingested.
  • UNII X687XDK09L
    A clay mineral processed to carry positive charges, used as a thickener and suspending agent in liquid medicines. It helps keep solid particles evenly distributed throughout the product.
  • UNII 420IP921MB
    A chelating agent derived from edetic acid that binds to metals in the formulation. It helps stabilize the medicine by preventing metal ions from causing breakdown or discoloration.
  • UNII 147D247K3P
    Ethylhexylglycerin is a synthetic preservative used to prevent bacteria and mold from growing in medicines and personal care products. It helps keep the product safe and stable throughout its shelf life.
  • UNII 14255EXE39
    Ethylparaben is a preservative, a chemical that stops bacteria and mold from growing in the medicine. It keeps the product safe and effective throughout its shelf life.
  • UNII 1K09F3G675
    Ferric oxide red is an inorganic iron compound used as a colorant in medicines. It gives tablets, capsules, or other dosage forms a red or reddish tint for identification and appearance.
  • UNII XM0M87F357
    A dark iron oxide compound that gives medicines their black or dark color. It's used as a colorant in tablets and capsules to help identify the product and make it visually distinctive.
  • UNII G7036X8B5H
    A dark iron compound that gives medicine its color. Used as a colorant in tablets and capsules to help identify the medication and make it visually distinctive.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII AVL0R9111T
    A plant extract from sea buckthorn berries. It's used in medicines as a natural coloring agent and flavor ingredient to make the product more appealing and easier to take.
  • UNII A8289P68Y2
    Isododecane is a lightweight liquid hydrocarbon used as a solvent and spreadability agent in topical formulations. It helps dissolve active ingredients and makes the product easier to apply and absorb into the skin.
  • UNII 113171Q70B
    Lauroyl lysine is a compound made by combining an amino acid (lysine) with a fatty acid (lauric acid). It works as a glidant and lubricant to help powder particles flow smoothly during manufacturing and tablet compression.
  • UNII ZYZ076G9JH
    Lens culinaris fruit is a plant-derived ingredient from lentil plants. It serves as a filler and source of plant-based material in formulations.
  • UNII DE08037SAB
    Magnesium sulfate is a mineral salt that acts as an osmotic agent in medications. It draws water into the intestines to soften stool or is used as a filler and processing aid in some solid dosage forms.
  • UNII 7CVR7L4A2D
    A starch-derived carbohydrate produced by breaking down corn, potato, or tapioca starch. It functions as a filler and binder to give the medicine bulk and texture, and sometimes as a mild sweetener or texture enhancer in powders and tablets.
  • UNII S73ZQI0GXM
    Methyl trimethicone is a silicone-based lubricant and glidant used in tablets and capsules. It reduces friction between particles and equipment during manufacturing, helping the medicine flow smoothly and compress evenly.
  • UNII A2I8C7HI9T
    Methylparaben is a preservative derived from benzoic acid that prevents growth of bacteria, fungi, and mold in medicines. It extends the product's shelf life and maintains safety during storage.
  • UNII HIE492ZZ3T
    Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
  • UNII 1VPU26JZZ4
    Potassium sorbate is a salt derived from sorbic acid, a naturally occurring preservative. It prevents growth of mold, yeast, and some bacteria, extending the medicine's shelf life.
  • UNII 8D08K3S51E
    Propylene carbonate is a clear liquid solvent derived from propylene. It helps dissolve or suspend active ingredients in liquid medicines and can improve how well the product flows and mixes.
  • UNII O4446S9CRA
    A synthetic oily liquid made from propylene glycol and fatty acids. It acts as a solvent and emulsifier to help dissolve or mix ingredients, and improves how the medicine spreads or absorbs in the body.
  • UNII M6S840WXG5
    Purslane is a plant-derived ingredient used in pharmaceuticals as a natural source of beneficial compounds. It functions as an antioxidant and anti-inflammatory agent to help stabilize the formula and support product shelf life.
  • UNII ETJ7Z6XBU4
    Silicon dioxide is a naturally occurring mineral used as a glidant and anti-caking agent. It helps powder ingredients flow smoothly and prevents clumping during manufacturing and storage.
  • UNII OJ245FE5EU
    Sodium benzoate is a salt derived from benzoic acid, a preservative. It's added to medicines to prevent growth of bacteria, fungi, and other microorganisms that could spoil the product.
  • UNII TU7HW0W0QT
    A salt derived from lactic acid, sodium lactate acts as a buffer and pH stabilizer in medicines. It helps maintain the product's acidity level and can also serve as a humectant to retain moisture.
  • UNII AYU7QD893W
    A naturally-derived amino acid compound used as an emulsifier and surfactant. It helps blend oil and water-based ingredients together and improves the product's texture and stability.
  • UNII 469OTG57A2
    Sodium pyrrolidone carboxylate is a synthetic polymer derived from pyrrolidone chemistry. It functions as a solubilizer and binder in medications, helping dissolve poorly water-soluble drugs and hold tablet ingredients together.
  • UNII X045WJ989B
    Sorbic acid is a preservative derived from berries that prevents mold, yeast, and bacterial growth in medicines. It keeps the product stable and safe during storage.
  • UNII 0W8RRI5W5A
    A fatty acid derivative used as an emulsifier and surfactant in medications. It helps blend oily and water-based ingredients together to create a stable, uniform product.
  • UNII 4ELV7Z65AP
    Stearic acid is a fatty acid derived from plant or animal sources. It acts as a binder and lubricant in tablets and capsules, helping them hold together and flow smoothly during manufacturing.
  • UNII LDC331P08E
    A silicone-based compound that acts as a glidant and flow agent in solid medications. It reduces friction between powder particles, helping the medicine flow smoothly during manufacturing and tablet compression.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.
  • UNII 231473QB6R
    Watermelon is a fruit extract or flavoring agent. It's added to medicines to improve taste, making the product more palatable, especially for children or medications with unpleasant flavors.
  • UNII SOI2LOH54Z
    Zinc oxide is a white mineral powder used in medicines as a protective barrier agent and color additive. It helps shield skin in topical products and may also serve as a filler or opacifying ingredient.

42 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesInactive (non-medicinal)ingredients Water (Aqua), Methy l Trimethicone, Propylene Glycol Dicaprylate/Dicaprate, Isododecane, C12-15 Alkyl Benzoate, Cetyl PEG/PPG-10/1 Dimethicone, Glycerin, HDI/Trimethylol Hexyllactone Crosspolymer, Silica, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Dimethicone, Magnesium Sulfate, Lauroyl Lysine, Tocopheryl Acetate, CitrullusLanatus (Watermelon) Fruit Extract, Lens Esculenta (Lentil) Fruit Extract, Pyrus Malus(Apple) Fruit Extract, Hippophae Rhamnoides Fruit Extract,Portulaca Oleracea Extract,Palmitoyl Tripeptide-38, Sodium PCA, Sodium Lactate,Sodium Ascorbyl Glucoside, Sodium Myristoyl Glutamate,Maltodextrin, Sorbitan Sesquioleate, Aluminum Hydroxide (CI 77002), Stearic Acid, Cyclopentasiloxane, Caprylyl Glycol, Zinc Oxide (CI 77947), Butylene Glycol, Ethylhexylglycerin, Acrylates/ Dimethicone Copolymer, Dimethicone/PEG-10/15 Crosspolymer, Triethoxycaprylylsilane, Sorbic Acid, Trisodium EDTA, Hydroxypropyl Cyclodextrin, Potassium Sorbate, Sodium Benzoate, Disteardimonium Hectorite, Propylene Carbonate, Phenoxyethanol, Methylparaben, Propylparaben, Ethylparaben, May Contain/ Peut Contenir (+/-), Iron Oxides (CI 77489, CI 77491, CI 77492, CI 77499), Titanium Dioxide (CI 77891).

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

💲 Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer gPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
CC Cream Broad Spectrum SPF 30 Merle Norman 7 g/100g; 2.5 g/100g; 2 g/100g; 4.1 g/100gthis 57627-0170-02 Merle 1 tube — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

⏳ Availability & generic status

🏛️
2014
On the market since
Jun 2014
📍
2026
Currently FDA-listed
12 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
57627-0170-02 You're viewing this 1 TUBE in 1 CARTON (57627-170-02) / 35 g in 1 TUBE (57627-170-01) 2014-06-19 Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product
What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos — Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured) ✓ Available
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The FDA registers it as 57627-170-02, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 57627-0170-02, written without dashes as 57627017002. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 57627-0170-02, the first segment (57627) is the labeler code FDA assigned to Merle Norman Cosmetics, Inc; the middle segment (0170) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (02) identifies this exact package size and type. Together they name one specific package of one specific product.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Merle Norman Cosmetics, Inc. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Merle Norman Cosmetics, Inc is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.

📄 FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage ~2 min read ▾

Stop use and ask a doctor if rash occurs. En cas de rougeurs cessez l'utilisationet consultez un medecin. Warnings For external use only Do not use on damaged or broken skin When using this product keep out of eyes.

Rinse with water to remove. If swallowed, get medical help or contact a Poison Control Center right away. Avertissements À usage externe seulement Ne pas utilisersur une peau abîmée ou des plaies ouvertes Faites attention à vos yeux lorsque vous utilisez ce produit.

Nettoyez avec de l’eau. Ne pas laisser à la portée des enfants. Si vous avalez ce produit, consultez un médecin ou contactez immédiatement un centre antipoison.

Drug Facts Directions • For sunscreen use: • apply liberally and evenly 15 minutes before sun exposure • use a water resistant sunscreen if swimming or sweating • reapply at least every 2 hours •Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: • limit time in the sun, especially from 10 a.m.-2 p.m. • wear long-sleeved shirts, pants, hats, and sunglasses • children under 6 months: Ask a doctor Mode d’emploi • Pour vous protéger de soleil: • appliquez généreusement et uniformément 15 minutes avant de vous mettre au soleil • utilisez un écran solaire résistant a l’eau si vous nagez ou transpirez • réappliquez au moins toutes les 2 heures • Mesures de protection contre le soleil.

L’exposition au soleil accroît le risque de cancer et de vieillissement prématuré de la peau. Pour amoindrir ce risque, utilisez régulièrement un écran solaire à ample protection FPS 15 ou plus et observez d’autres mesures de protection contre le soleil telles que: • limiter le temps d’exposition au soleil, surtout entre 10 heures et 14 heures • porter des chemises à manches longues, des pantalons, des chapeaux et des lunettes de soleil • pour les enfants de moins de 6 mois: Consulter un médecin Inactive (non-medicinal)ingredients Water (Aqua), Methy l Trimethicone, Propylene Glycol Dicaprylate/Dicaprate, Isododecane, C12-15 Alkyl Benzoate, Cetyl PEG/PPG-10/1 Dimethicone, Glycerin, HDI/Trimethylol Hexyllactone Crosspolymer, Silica, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Dimethicone, Magnesium Sulfate, Lauroyl Lysine, Tocopheryl Acetate, CitrullusLanatus (Watermelon) Fruit Extract, Lens Esculenta (Lentil) Fruit Extract, Pyrus Malus(Apple) Fruit Extract, Hippophae Rhamnoides Fruit Extract,Portulaca Oleracea Extract,Palmitoyl Tripeptide-38, Sodium PCA, Sodium Lactate,Sodium Ascorbyl Glucoside, Sodium Myristoyl Glutamate,Maltodextrin, Sorbitan Sesquioleate, Aluminum Hydroxide (CI 77002), Stearic Acid, Cyclopentasiloxane, Caprylyl Glycol, Zinc Oxide (CI 77947), Butylene Glycol, Ethylhexylglycerin, Acrylates/ Dimethicone Copolymer, Dimethicone/PEG-10/15 Crosspolymer, Triethoxycaprylylsilane, Sorbic Acid, Trisodium EDTA, Hydroxypropyl Cyclodextrin, Potassium Sorbate, Sodium Benzoate, Disteardimonium Hectorite, Propylene Carbonate, Phenoxyethanol, Methylparaben, Propylparaben, Ethylparaben, May Contain/ Peut Contenir (+/-), Iron Oxides (CI 77489, CI 77491, CI 77492, CI 77499), Titanium Dioxide (CI 77891).

⏱️ Dosage and Administration ~2 min read ▾

Drug Facts Directions • For sunscreen use: • apply liberally and evenly 15 minutes before sun exposure • use a water resistant sunscreen if swimming or sweating • reapply at least every 2 hours •Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: • limit time in the sun, especially from 10 a.m.-2 p.m. • wear long-sleeved shirts, pants, hats, and sunglasses • children under 6 months: Ask a doctor Mode d’emploi • Pour vous protéger de soleil: • appliquez généreusement et uniformément 15 minutes avant de vous mettre au soleil • utilisez un écran solaire résistant a l’eau si vous nagez ou transpirez • réappliquez au moins toutes les 2 heures • Mesures de protection contre le soleil.

L’exposition au soleil accroît le risque de cancer et de vieillissement prématuré de la peau. Pour amoindrir ce risque, utilisez régulièrement un écran solaire à ample protection FPS 15 ou plus et observez d’autres mesures de protection contre le soleil telles que: • limiter le temps d’exposition au soleil, surtout entre 10 heures et 14 heures • porter des chemises à manches longues, des pantalons, des chapeaux et des lunettes de soleil • pour les enfants de moins de 6 mois: Consulter un médecin Inactive (non-medicinal)ingredients Water (Aqua), Methy l Trimethicone, Propylene Glycol Dicaprylate/Dicaprate, Isododecane, C12-15 Alkyl Benzoate, Cetyl PEG/PPG-10/1 Dimethicone, Glycerin, HDI/Trimethylol Hexyllactone Crosspolymer, Silica, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Dimethicone, Magnesium Sulfate, Lauroyl Lysine, Tocopheryl Acetate, CitrullusLanatus (Watermelon) Fruit Extract, Lens Esculenta (Lentil) Fruit Extract, Pyrus Malus(Apple) Fruit Extract, Hippophae Rhamnoides Fruit Extract,Portulaca Oleracea Extract,Palmitoyl Tripeptide-38, Sodium PCA, Sodium Lactate,Sodium Ascorbyl Glucoside, Sodium Myristoyl Glutamate,Maltodextrin, Sorbitan Sesquioleate, Aluminum Hydroxide (CI 77002), Stearic Acid, Cyclopentasiloxane, Caprylyl Glycol, Zinc Oxide (CI 77947), Butylene Glycol, Ethylhexylglycerin, Acrylates/ Dimethicone Copolymer, Dimethicone/PEG-10/15 Crosspolymer, Triethoxycaprylylsilane, Sorbic Acid, Trisodium EDTA, Hydroxypropyl Cyclodextrin, Potassium Sorbate, Sodium Benzoate, Disteardimonium Hectorite, Propylene Carbonate, Phenoxyethanol, Methylparaben, Propylparaben, Ethylparaben, May Contain/ Peut Contenir (+/-), Iron Oxides (CI 77489, CI 77491, CI 77492, CI 77499), Titanium Dioxide (CI 77891).

⚠️ Warnings ~2 min read ▾

Warnings For external use only Do not use on damaged or broken skin When using this product keep out of eyes. Rinse with water to remove. If swallowed, get medical help or contact a Poison Control Center right away.

Avertissements À usage externe seulement Ne pas utilisersur une peau abîmée ou des plaies ouvertes Faites attention à vos yeux lorsque vous utilisez ce produit. Nettoyez avec de l’eau. Ne pas laisser à la portée des enfants.

Si vous avalez ce produit, consultez un médecin ou contactez immédiatement un centre antipoison. Drug Facts Directions • For sunscreen use: • apply liberally and evenly 15 minutes before sun exposure • use a water resistant sunscreen if swimming or sweating • reapply at least every 2 hours •Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging.

To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: • limit time in the sun, especially from 10 a.m.-2 p.m. • wear long-sleeved shirts, pants, hats, and sunglasses • children under 6 months: Ask a doctor Mode d’emploi • Pour vous protéger de soleil: • appliquez généreusement et uniformément 15 minutes avant de vous mettre au soleil • utilisez un écran solaire résistant a l’eau si vous nagez ou transpirez • réappliquez au moins toutes les 2 heures • Mesures de protection contre le soleil.

L’exposition au soleil accroît le risque de cancer et de vieillissement prématuré de la peau. Pour amoindrir ce risque, utilisez régulièrement un écran solaire à ample protection FPS 15 ou plus et observez d’autres mesures de protection contre le soleil telles que: • limiter le temps d’exposition au soleil, surtout entre 10 heures et 14 heures • porter des chemises à manches longues, des pantalons, des chapeaux et des lunettes de soleil • pour les enfants de moins de 6 mois: Consulter un médecin Inactive (non-medicinal)ingredients Water (Aqua), Methy l Trimethicone, Propylene Glycol Dicaprylate/Dicaprate, Isododecane, C12-15 Alkyl Benzoate, Cetyl PEG/PPG-10/1 Dimethicone, Glycerin, HDI/Trimethylol Hexyllactone Crosspolymer, Silica, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Dimethicone, Magnesium Sulfate, Lauroyl Lysine, Tocopheryl Acetate, CitrullusLanatus (Watermelon) Fruit Extract, Lens Esculenta (Lentil) Fruit Extract, Pyrus Malus(Apple) Fruit Extract, Hippophae Rhamnoides Fruit Extract,Portulaca Oleracea Extract,Palmitoyl Tripeptide-38, Sodium PCA, Sodium Lactate,Sodium Ascorbyl Glucoside, Sodium Myristoyl Glutamate,Maltodextrin, Sorbitan Sesquioleate, Aluminum Hydroxide (CI 77002), Stearic Acid, Cyclopentasiloxane, Caprylyl Glycol, Zinc Oxide (CI 77947), Butylene Glycol, Ethylhexylglycerin, Acrylates/ Dimethicone Copolymer, Dimethicone/PEG-10/15 Crosspolymer, Triethoxycaprylylsilane, Sorbic Acid, Trisodium EDTA, Hydroxypropyl Cyclodextrin, Potassium Sorbate, Sodium Benzoate, Disteardimonium Hectorite, Propylene Carbonate, Phenoxyethanol, Methylparaben, Propylparaben, Ethylparaben, May Contain/ Peut Contenir (+/-), Iron Oxides (CI 77489, CI 77491, CI 77492, CI 77499), Titanium Dioxide (CI 77891).

🧪 Active Ingredient ~3 min read ▾

Active (medicinal) Ingredients (w/w) Purpose Homosalate 7.0% Sunscreen Octinoxate 2.5% Sunscreen Oxybenzone 2.0% Sunscreen Titanium Dioxide 4.1% Sunscreen Uses • helps prevent sunburn • if used as directed withother sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun Utilisations • aide à prévenir les coups de soleil • amoindrit le risque de cancer et de vieillissement prématuré de la peau causés par le soleil lorsque utilisé comme indiqué en conjonction avec d’autres mesures de protection solaire (voir Mode d’emploi).

Keep out of reach of children Stop use and ask a doctor if rash occurs. En cas de rougeurs cessez l'utilisationet consultez un medecin. Warnings For external use only Do not use on damaged or broken skin When using this product keep out of eyes.

Rinse with water to remove. If swallowed, get medical help or contact a Poison Control Center right away. Avertissements À usage externe seulement Ne pas utilisersur une peau abîmée ou des plaies ouvertes Faites attention à vos yeux lorsque vous utilisez ce produit.

Nettoyez avec de l’eau. Ne pas laisser à la portée des enfants. Si vous avalez ce produit, consultez un médecin ou contactez immédiatement un centre antipoison.

Drug Facts Directions • For sunscreen use: • apply liberally and evenly 15 minutes before sun exposure • use a water resistant sunscreen if swimming or sweating • reapply at least every 2 hours •Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: • limit time in the sun, especially from 10 a.m.-2 p.m. • wear long-sleeved shirts, pants, hats, and sunglasses • children under 6 months: Ask a doctor Mode d’emploi • Pour vous protéger de soleil: • appliquez généreusement et uniformément 15 minutes avant de vous mettre au soleil • utilisez un écran solaire résistant a l’eau si vous nagez ou transpirez • réappliquez au moins toutes les 2 heures • Mesures de protection contre le soleil.

L’exposition au soleil accroît le risque de cancer et de vieillissement prématuré de la peau. Pour amoindrir ce risque, utilisez régulièrement un écran solaire à ample protection FPS 15 ou plus et observez d’autres mesures de protection contre le soleil telles que: • limiter le temps d’exposition au soleil, surtout entre 10 heures et 14 heures • porter des chemises à manches longues, des pantalons, des chapeaux et des lunettes de soleil • pour les enfants de moins de 6 mois: Consulter un médecin Inactive (non-medicinal)ingredients Water (Aqua), Methy l Trimethicone, Propylene Glycol Dicaprylate/Dicaprate, Isododecane, C12-15 Alkyl Benzoate, Cetyl PEG/PPG-10/1 Dimethicone, Glycerin, HDI/Trimethylol Hexyllactone Crosspolymer, Silica, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Dimethicone, Magnesium Sulfate, Lauroyl Lysine, Tocopheryl Acetate, CitrullusLanatus (Watermelon) Fruit Extract, Lens Esculenta (Lentil) Fruit Extract, Pyrus Malus(Apple) Fruit Extract, Hippophae Rhamnoides Fruit Extract,Portulaca Oleracea Extract,Palmitoyl Tripeptide-38, Sodium PCA, Sodium Lactate,Sodium Ascorbyl Glucoside, Sodium Myristoyl Glutamate,Maltodextrin, Sorbitan Sesquioleate, Aluminum Hydroxide (CI 77002), Stearic Acid, Cyclopentasiloxane, Caprylyl Glycol, Zinc Oxide (CI 77947), Butylene Glycol, Ethylhexylglycerin, Acrylates/ Dimethicone Copolymer, Dimethicone/PEG-10/15 Crosspolymer, Triethoxycaprylylsilane, Sorbic Acid, Trisodium EDTA, Hydroxypropyl Cyclodextrin, Potassium Sorbate, Sodium Benzoate, Disteardimonium Hectorite, Propylene Carbonate, Phenoxyethanol, Methylparaben, Propylparaben, Ethylparaben, May Contain/ Peut Contenir (+/-), Iron Oxides (CI 77489, CI 77491, CI 77492, CI 77499), Titanium Dioxide (CI 77891).

🧪 Inactive Ingredients 123 words ▾

Inactive (non-medicinal)ingredients Water (Aqua), Methy l Trimethicone, Propylene Glycol Dicaprylate/Dicaprate, Isododecane, C12-15 Alkyl Benzoate, Cetyl PEG/PPG-10/1 Dimethicone, Glycerin, HDI/Trimethylol Hexyllactone Crosspolymer, Silica, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Dimethicone, Magnesium Sulfate, Lauroyl Lysine, Tocopheryl Acetate, CitrullusLanatus (Watermelon) Fruit Extract, Lens Esculenta (Lentil) Fruit Extract, Pyrus Malus(Apple) Fruit Extract, Hippophae Rhamnoides Fruit Extract,Portulaca Oleracea Extract,Palmitoyl Tripeptide-38, Sodium PCA, Sodium Lactate,Sodium Ascorbyl Glucoside, Sodium Myristoyl Glutamate,Maltodextrin, Sorbitan Sesquioleate, Aluminum Hydroxide (CI 77002), Stearic Acid, Cyclopentasiloxane, Caprylyl Glycol, Zinc Oxide (CI 77947), Butylene Glycol, Ethylhexylglycerin, Acrylates/ Dimethicone Copolymer, Dimethicone/PEG-10/15 Crosspolymer, Triethoxycaprylylsilane, Sorbic Acid, Trisodium EDTA, Hydroxypropyl Cyclodextrin, Potassium Sorbate, Sodium Benzoate, Disteardimonium Hectorite, Propylene Carbonate, Phenoxyethanol, Methylparaben, Propylparaben, Ethylparaben, May Contain/ Peut Contenir (+/-), Iron Oxides (CI 77489, CI 77491, CI 77492, CI 77499), Titanium Dioxide (CI 77891).

🎯 Purpose ~2 min read ▾

Uses • helps prevent sunburn • if used as directed withother sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun Utilisations • aide à prévenir les coups de soleil • amoindrit le risque de cancer et de vieillissement prématuré de la peau causés par le soleil lorsque utilisé comme indiqué en conjonction avec d’autres mesures de protection solaire (voir Mode d’emploi). Keep out of reach of children Stop use and ask a doctor if rash occurs. En cas de rougeurs cessez l'utilisationet consultez un medecin.

Warnings For external use only Do not use on damaged or broken skin When using this product keep out of eyes. Rinse with water to remove. If swallowed, get medical help or contact a Poison Control Center right away.

Avertissements À usage externe seulement Ne pas utilisersur une peau abîmée ou des plaies ouvertes Faites attention à vos yeux lorsque vous utilisez ce produit. Nettoyez avec de l’eau. Ne pas laisser à la portée des enfants.

Si vous avalez ce produit, consultez un médecin ou contactez immédiatement un centre antipoison. Drug Facts Directions • For sunscreen use: • apply liberally and evenly 15 minutes before sun exposure • use a water resistant sunscreen if swimming or sweating • reapply at least every 2 hours •Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging.

To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: • limit time in the sun, especially from 10 a.m.-2 p.m. • wear long-sleeved shirts, pants, hats, and sunglasses • children under 6 months: Ask a doctor Mode d’emploi • Pour vous protéger de soleil: • appliquez généreusement et uniformément 15 minutes avant de vous mettre au soleil • utilisez un écran solaire résistant a l’eau si vous nagez ou transpirez • réappliquez au moins toutes les 2 heures • Mesures de protection contre le soleil.

L’exposition au soleil accroît le risque de cancer et de vieillissement prématuré de la peau. Pour amoindrir ce risque, utilisez régulièrement un écran solaire à ample protection FPS 15 ou plus et observez d’autres mesures de protection contre le soleil telles que: • limiter le temps d’exposition au soleil, surtout entre 10 heures et 14 heures • porter des chemises à manches longues, des pantalons, des chapeaux et des lunettes de soleil • pour les enfants de moins de 6 mois: Consulter un médecin Inactive (non-medicinal)ingredients Water (Aqua), Methy l Trimethicone, Propylene Glycol Dicaprylate/Dicaprate, Isododecane, C12-15 Alkyl Benzoate, Cetyl PEG/PPG-10/1 Dimethicone, Glycerin, HDI/Trimethylol Hexyllactone Crosspolymer, Silica, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Dimethicone, Magnesium Sulfate, Lauroyl Lysine, Tocopheryl Acetate, CitrullusLanatus (Watermelon) Fruit Extract, Lens Esculenta (Lentil) Fruit Extract, Pyrus Malus(Apple) Fruit Extract, Hippophae Rhamnoides Fruit Extract,Portulaca Oleracea Extract,Palmitoyl Tripeptide-38, Sodium PCA, Sodium Lactate,Sodium Ascorbyl Glucoside, Sodium Myristoyl Glutamate,Maltodextrin, Sorbitan Sesquioleate, Aluminum Hydroxide (CI 77002), Stearic Acid, Cyclopentasiloxane, Caprylyl Glycol, Zinc Oxide (CI 77947), Butylene Glycol, Ethylhexylglycerin, Acrylates/ Dimethicone Copolymer, Dimethicone/PEG-10/15 Crosspolymer, Triethoxycaprylylsilane, Sorbic Acid, Trisodium EDTA, Hydroxypropyl Cyclodextrin, Potassium Sorbate, Sodium Benzoate, Disteardimonium Hectorite, Propylene Carbonate, Phenoxyethanol, Methylparaben, Propylparaben, Ethylparaben, May Contain/ Peut Contenir (+/-), Iron Oxides (CI 77489, CI 77491, CI 77492, CI 77499), Titanium Dioxide (CI 77891).

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
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For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.