Home › NDC Lookup › Ingredients › Octinoxate, Octisalate, Oxybenzone, And... › 72203-0010-01
COVER plus CORRECT/TINTED MOISTURIZER CC CRM GOLDEN LIGHT Octinoxate, Octisalate, Oxybenzone, and Titanium Dioxide 75 mg/g; 50 mg/g; 30 mg/g; 67.4 mg/g Cream — NDC 72203-0010-01 package photo

COVER plus CORRECT/TINTED MOISTURIZER CC CRM GOLDEN LIGHT Octinoxate, Octisalate, Oxybenzone, and Titanium Dioxide 75 mg/g; 50 mg/g; 30 mg/g; 67.4 mg/g Cream

by Bluemercury · 1 TUBE in 1 CARTON (72203-010-01) / 50 g in 1 TUBE
NDC 72203-0010-01
🏷️ FDA NDC (as labeled) 72203-010-01 billing pads the product segment with a zero
OTC On market Non-controlled
🗂️ Data synced Sep 10, 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) 72203-010-01
Product NDC 72203-010
11-digit billing NDC 72203001001
UNII 4Y5P7MUD51, 15FIX9V2JP, 4X49Y0596W, 95OOS7VE0Y
UPC 0814309020221
Application # M020
SPL Set ID 5c590aed-d2f2-4478-8919-37c848752b42
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2015-08-20
Route TOPICAL
Dosage form CREAM
Substance OCTINOXATE; OCTISALATE; OXYBENZONE; TITANIUM DIOXIDE
Why two NDCs? The FDA registers this code as 72203-010-01 — 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 → 72203-0010-01. 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

LabelerBluemercury
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code72203
First marketedAug 2015
Product typeHuman Otc Drug
Portfolio11 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 tinted moisturizer cream applied to the skin that contains four active sunscreen ingredients. Octinoxate, octisalate, and oxybenzone function as chemical UV filters that absorb ultraviolet rays, while titanium dioxide is a mineral UV filter that reflects and scatters those rays. Together, these ingredients are combined in this cream to provide broad-spectrum sun protection in a moisturizing base. As an OTC monograph product, it is marketed under FDA's established rule-book for sunscreens rather than as an individually reviewed drug 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 K72T3FS567
    Adenosine is a naturally occurring nucleoside compound. In medicines, it functions as an active pharmaceutical ingredient in some formulations, though when listed as an excipient it may serve as a buffering or stabilizing agent to maintain product stability and pH.
  • UNII 344S277G0Z
    Allantoin is a naturally derived compound that helps soften and soothe skin. In medicines, it works as a skin-conditioning agent and may help support wound healing and reduce irritation in topical formulations.
  • UNII G4888SY0QO
    Aminoethylphosphinic acid is a synthetic organic compound used as a chelating agent or buffering substance in medications. It helps stabilize the drug formulation and may improve how the active ingredient stays effective in the product.
  • UNII LU49E6626Q
    A synthetic organic compound used as a pH buffer and neutralizing agent in medicines. It helps maintain the proper acidity level in liquid formulations to improve stability and comfort.
  • UNII 9TLV70SV6I
    A natural essential oil extracted from bitter orange peel, used as a flavoring agent to mask unpleasant tastes and improve the palatability of medicines.
  • 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 68103A23TQ
    A synthetic cleansing agent made from plant oils and ethylene oxide. It helps mix oil and water based ingredients together and allows the medicine to spread evenly on skin.
  • 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 Q95M2P1KJL
    A silicone-based ingredient that acts as a lubricant and glidant. It helps the tablet or capsule move smoothly through manufacturing equipment and improves powder flow during production.
  • UNII K679OBS311
    Carboxymethylcellulose sodium is a plant-derived thickening agent made from cellulose. In medicines, it acts as a binder to hold ingredients together, a disintegrant to help the tablet break apart, or a thickener in liquids.
  • UNII S57M60MI88
    A synthetic liquid preservative and humectant derived from petroleum. It helps prevent microbial growth and keeps the product moist, commonly used in topical medications and cosmetic formulations.
  • 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 E107L85C40
    Dipropylene glycol is a clear liquid made from propylene glycol. It acts as a solvent and humectant in medicines, helping dissolve active ingredients and retain moisture in the formulation.
  • UNII 8NLQ36F6MM
    Edetate disodium anhydrous is a chemical compound that binds to metal ions in a medicine. It's used as a stabilizer to prevent unwanted chemical reactions and help keep the drug product effective during storage.
  • 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 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 EX438O2MRT
    Ferric oxide yellow is a naturally occurring iron compound used as a colorant in medications. It gives tablets, capsules, and other forms a yellow or golden hue 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 NNE56F2N14
    A synthetic compound derived from glycerin and polyethylene glycol. It acts as an emulsifier and solubilizer to help mix water and oil-based ingredients and keep them blended throughout the product's shelf life.
  • 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 CA2Y0FE3FX
    A salt derived from licorice root extract, used as a flavoring agent and sweetener. It may also help soothe and protect mucous membranes in throat lozenges and cough products.
  • UNII UG00KM4WR7
    A plastic polymer used as a container material and film coating. It helps protect the medicine from moisture and air exposure during storage and shipping.
  • UNII YSE9PPT4TH
    Hyaluronate sodium is a natural carbohydrate that holds moisture. It's used in medicines as a lubricant, thickener, and moisture-retaining agent to improve texture and delivery of the active ingredient.
  • UNII 918X1OUF1E
    Isohexadecane is a synthetic hydrocarbon oil used as an emollient and solvent in topical medicines. It helps dissolve active ingredients and improves spreadability and absorption through the skin.
  • UNII V8A1AW0880
    Mica is a naturally occurring mineral that's ground into fine powder. It's used in medicines as a colorant and anti-caking agent to improve appearance and prevent clumping in tablets or powders.
  • UNII 77T908SE82
    Neopentyl glycol dicaprate is a synthetic oily compound used as an emollient and skin-conditioning agent in topical formulations. It helps soften and smooth the product's texture while improving how it spreads on skin.
  • UNII GIA7T764OD
    A silicone-based ingredient combined with polyethylene glycol. It acts as an emulsifier and surfactant to help blend oils and water-based ingredients, and reduces foaming in liquid formulations.
  • 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 DR0K5NOJ4R
    Phenyl trimethicone is a silicone-based lubricant and glidant. It helps powder particles flow smoothly and reduces friction during tablet or capsule manufacturing and filling.
  • UNII 1212Z7S33A
    PEG-32 is a synthetic polymer derived from ethylene oxide. It acts as a humectant and solvent in medications, helping to dissolve or suspend active ingredients and maintain moisture in solid dosage forms.
  • UNII CAL22UVI4M
    A synthetic emulsifier derived from sorbitol and fatty acids. It helps mix oil and water-based ingredients together and improves the texture and stability of the medicine.
  • UNII 03KCY6P7UT
    A waxy compound derived from cetyl alcohol and phosphoric acid. It acts as an emulsifier to help blend oil and water ingredients, and as a thickener to give the medicine its proper texture and consistency.
  • 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 506T60A25R
    Sorbitol is a natural sugar alcohol derived from glucose. It serves as a sweetener, humectant, and bulking agent in medications to improve taste and help maintain moisture in the product.
  • UNII 53J3F32P58
    A synthetic detergent derived from stearic acid, a fatty substance. It helps dissolve or distribute oil-based ingredients evenly throughout the medicine, acting as an emulsifier and solubilizer in tablets and capsules.
  • UNII 2KR89I4H1Y
    Stearyl alcohol is a waxy, fatty substance derived from natural oils or made synthetically. It acts as an emulsifier and thickener in medicines, helping mix ingredients together and give the product the right texture.
  • 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.

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

The official label also statesWater (Aqua), Phenyl Trimethicone, Neopentyl Glycol Dicaprate, Butylene Glycol, Glycerin, C20-40 Pareth-3, Caprylyl Methicone, Steareth-21, Glycereth-26, Dipropylene Glycol, PEG-8 Dimethicone, Silica, Tocopheryl Acetate, Sodium Hyaluronate, Citrus Aurantium Amara (Bitter Orange) Peel Oil, Dimethicone, Phenoxyethanol, Potassium Cetyl Phosphate, Stearyl Alcohol, Trimethylsiloxysilicate, Caprylyl Glycol, Mica, PEG-32, Polypropylsilsesquioxane, VP/Eicosene Copolymer, Polyethylene, Hydroxyethyl Acrylate/Sodium Accryloyldimethyl Taurate Copolymer, Hydrolyzed Wheat Protein/PVP Crosspolymer, Sorbitol, Decylene Glycol, Isohexadecane, Steareth-21, Cellulose Gum, Allantoin, Dipotassium Glycyrrhizate, Disodium EDTA, Polysorbate 60, Adenosine, Aminomethyl Propanol, Aminoethylphosphinic Acid, Hippophae Rhamnoides oil, Palmaria Palmata Extract, Cichorium Intybus (Chicory) Root Extract, Ethylhexylglycerin, Lecithin, Ammonium Polyacrylate, Iron Oxides (CI 77492), Iron Oxides (CI 77491), Iron Oxides (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
COVER plus CORRECT/TINTED MOISTURIZER CC CRM LIGHT 75 mg/g; 50 mg/g; 30 mg/g; 67.4 mg/g 72203-0006-01 Bluemercury 1 tube — — FDA listed —
COVER plus CORRECT/TINTED MOISTURIZER CC CRM GOLDEN LIGHT 75 mg/g; 50 mg/g; 30 mg/g; 67.4 mg/gthis 72203-0010-01 Bluemercury 1 tube — — FDA listed —
COVER plus CORRECT/TINTED MOISTURIZER CC CRM MED 75 mg/g; 50 mg/g; 30 mg/g; 67.4 mg/g 72203-0007-01 Bluemercury 1 tube — — FDA listed —
COVER plus CORRECT/TINTED MOISTURIZER CC CRM MED/DEEP 75 mg/g; 50 mg/g; 30 mg/g; 67.4 mg/g 72203-0008-01 Bluemercury 1 tube — — FDA listed —
COVER plus CORRECT/TINTED MOISTURIZER CC CRM PORCELAIN 75 mg/g; 50 mg/g; 30 mg/g; 67.4 mg/g 72203-0009-01 Bluemercury 1 tube — — FDA listed —
COVER plus CORRECT/TINTED MOISTURIZER CC CRM FAIR 75 mg/g; 50 mg/g; 30 mg/g; 67.4 mg/g 72203-0005-01 Bluemercury 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

🏛️
2015
On the market since
Aug 2015
📍
2026
Currently FDA-listed
11 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
72203-0010-01 You're viewing this 1 TUBE in 1 CARTON (72203-010-01) / 50 g in 1 TUBE 2015-08-20 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 ✓ Available
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 72203-010-01, 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: 72203-0010-01, written without dashes as 72203001001. 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 72203-0010-01, the first segment (72203) is the labeler code FDA assigned to Bluemercury; the middle segment (0010) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) 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 Bluemercury. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Bluemercury 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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 30 words ▾

Uses Helps prevent sunburn. If used as directed with other sun protection measures (see Directions ), decreases the risk of skin cancer and early skin aging caused by the sun.

⏱️ Dosage and Administration 90 words ▾

Directions Apply liberally 15 minutes before sun exposure. Reapply at least every 2 hours. Use a water resistant sunscreen if swimming or sweating.

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 of 15 or higher and other sun protection measure including: Limit time in the sun, especially from 10am - 2pm.

Wear long-sleeve shirts, pants, hats and sunglasses. Children under 6 months of age: Ask a doctor.

⚠️ Warnings 54 words ▾

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. Stop use and ask a doctor if rash occurs. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

📦 Storage and Handling 14 words ▾

Other Information Protect the product in this container from excessive heat and direct sun.

🧪 Active Ingredient 16 words ▾

Active Ingredients Purpose Octinoxate 7.5% sunscreen Octisalate 5% sunscreen Oxybenzone 3% sunscreen Titanium Dioxide 6.74% sunscreen

🧪 Inactive Ingredients 109 words ▾

Inactive ingredients Water (Aqua), Phenyl Trimethicone, Neopentyl Glycol Dicaprate, Butylene Glycol, Glycerin, C20-40 Pareth-3, Caprylyl Methicone, Steareth-21, Glycereth-26, Dipropylene Glycol, PEG-8 Dimethicone, Silica, Tocopheryl Acetate, Sodium Hyaluronate, Citrus Aurantium Amara (Bitter Orange) Peel Oil, Dimethicone, Phenoxyethanol, Potassium Cetyl Phosphate, Stearyl Alcohol, Trimethylsiloxysilicate, Caprylyl Glycol, Mica, PEG-32, Polypropylsilsesquioxane, VP/Eicosene Copolymer, Polyethylene, Hydroxyethyl Acrylate/Sodium Accryloyldimethyl Taurate Copolymer, Hydrolyzed Wheat Protein/PVP Crosspolymer, Sorbitol, Decylene Glycol, Isohexadecane, Steareth-21, Cellulose Gum, Allantoin, Dipotassium Glycyrrhizate, Disodium EDTA, Polysorbate 60, Adenosine, Aminomethyl Propanol, Aminoethylphosphinic Acid, Hippophae Rhamnoides oil, Palmaria Palmata Extract, Cichorium Intybus (Chicory) Root Extract, Ethylhexylglycerin, Lecithin, Ammonium Polyacrylate, Iron Oxides (CI 77492), Iron Oxides (CI 77491), Iron Oxides (CI 77499), Titanium Dioxide (CI 77891)

🎯 Purpose 16 words ▾

Active Ingredients Purpose Octinoxate 7.5% sunscreen Octisalate 5% sunscreen Oxybenzone 3% sunscreen Titanium Dioxide 6.74% sunscreen

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 72203-0009-01 · Bluemercury 72203-0014-01 · Bluemercury →
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.