Home › NDC Lookup › Ingredients › Avobenzone Homosalate Octocrylene › 69968-0852-01
Neutrogena MoistureShine Lip Soother with Sunscreen SPF 20, Glow 70 Avobenzone, Homosalate, Octocrylene 100 mg/g; 100 mg/g; 30 mg/g Gel, 10 g — NDC 69968-0852-01 package photo

Neutrogena MoistureShine Lip Soother with Sunscreen SPF 20, Glow 70 Avobenzone, Homosalate, Octocrylene 100 mg/g; 100 mg/g; 30 mg/g Gel, 10 g

by Kenvue Brands LLC · 10 g in 1 TUBE (69968-0852-1)
NDC 69968-0852-01
🏷️ FDA NDC (as labeled) 69968-0852-1 billing pads the package segment with a zero
OTC On market Non-controlled
🗂️ Data synced Sep 17, 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) 69968-0852-1
Product NDC 69968-0852
11-digit billing NDC 69968085201
UNII G63QQF2NOX, V06SV4M95S, 5A68WGF6WM
UPC 0086800000914, 0086800000921, 0086800000938, 0086800690030
Application # M020
SPL Set ID 129ae274-0094-be5e-e063-6394a90a9801
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-04-11
Route TOPICAL
Dosage form GEL
Substance HOMOSALATE; OCTOCRYLENE; AVOBENZONE
Why two NDCs? The FDA registers this code as 69968-0852-1 — a 5-4-1 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 package segment → 69968-0852-01. 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

LabelerKenvue Brands LLC
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code69968
First marketedApr 2024
Product typeHuman Otc Drug
Portfolio564 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?

Neutrogena MoistureShine Lip Soother with Sunscreen SPF 20 is a topical gel marketed as an over-the-counter monograph product. It contains three active sunscreen ingredients: avobenzone, homosalate, and octocrylene, which are ultraviolet light absorbers typically used in lip balms and sunscreens to help protect skin from sun damage. This product is formulated to function as both a lip moisturizer and a sunscreen applied directly to the lips.

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 ZY81Z83H0X
    Aloe vera leaf is a plant extract derived from the aloe plant. It is used in medicines as a natural moisturizer and skin-soothing agent in topical formulations.
  • UNII QN83US2B0N
    Ascorbyl palmitate is a fat-soluble form of vitamin C used as an antioxidant in medicines. It prevents oils and fats in the product from breaking down and becoming less stable over time.
  • UNII 6L246LAM9T
    A synthetic oil derived from glycerol and adipic acid. It acts as an emulsifier and solubilizer in medicines, helping mix ingredients that don't naturally blend together and improving how the body absorbs the active drug.
  • UNII D5340Y2I9G
    Castor oil is a natural plant-based oil used in medicines as a lubricant, laxative agent, and solvent. It helps medicine ingredients dissolve or flow smoothly and can aid bowel movement in formulations designed for that purpose.
  • UNII FGL3685T2X
    Chamomile is a plant extract used in medications as a flavoring agent and for its mild soothing properties in formulations. It helps improve taste and aroma of the medicine.
  • UNII YY7C30VXJT
    A natural plant extract from cucumber that adds flavor and freshness to medicines. It may also serve as a moisturizing agent or mild preservative in topical or oral formulations.
  • UNII ECW0LZ41X8
    A synthetic red dye used to color tablets and capsules. It helps make medicines visually distinctive so patients can easily identify their medication.
  • UNII 1116DS0SNT
    A synthetic oily liquid used as a plasticizer and lubricant in tablets and capsules. It helps soften and increase flexibility of coatings while reducing friction during manufacturing and handling.
  • UNII 9G1OE216XY
    Docosanol is a waxy, fatty alcohol derived from plant sources. It acts as an emollient and thickener in topical medicines, helping to soften the skin and improve product texture and stability.
  • UNII J9EQA3S2JM
    FD&C Blue No. 1 Aluminum Lake is a blue colorant made by combining FD&C Blue No. 1 dye with aluminum salts. It is used to color tablets, capsules, and other medicines for easy identification and appearance.
  • 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 L7T10EIP3A
    A cooling compound from mint plants used as a flavoring agent and to create a fresh sensation in medicines. It helps mask bitter tastes and improve how the product feels in the mouth.
  • UNII 461N1O614Y
    A synthetic oily liquid used as an emollient and solvent in medications. It helps dissolve active ingredients and improves how the medicine spreads or absorbs through the skin.
  • UNII 255PIF62MS
    A synthetic antioxidant compound used to prevent oils and fats in medications from breaking down or becoming rancid during storage. It helps maintain the medicine's stability and shelf life.
  • UNII 1NA5AO9GH7
    A synthetic polymer derived from petroleum, polybutene is used as a binder and lubricant in solid medications to help hold ingredients together and improve the tablet or capsule's flow during manufacturing.
  • UNII 8FDA8C98S3
    A plant-derived thickening and emulsifying agent that helps blend oil and water-based ingredients together. Used in topical formulations to create stable, smooth textures.
  • UNII FST467XS7D
    Saccharin is an artificial sweetener derived from benzoic sulfinilanide. It's added to medicines to improve taste and make them easier to take, especially in liquid or chewable formulations.
  • UNII 68CMP2MB55
    A brown seaweed extract used as a thickener and stabilizer in liquid medicines and suspensions. It helps maintain consistent texture and prevents ingredients from separating.
  • UNII 65UEH262IS
    Safflower oil is a plant-based oil extracted from safflower seeds. It's used in medicines as a solvent and carrier to help dissolve or suspend active ingredients, and sometimes as an emollient to improve texture.
  • UNII 241ATL177A
    Soybean oil is a natural plant oil derived from soybean seeds. It's used in medicines as a solvent and carrier to help dissolve or suspend active ingredients and improve how the body absorbs them.
  • UNII 9K7IG15M0Q
    Arthrospira maxima is a blue-green algae (spirulina) used as a natural colorant and nutritional ingredient in medicines. It adds blue-green color to tablets and capsules while providing vitamins and minerals.
  • UNII KM7N50LOS6
    Tin oxide is an inorganic mineral compound used in medicines as a colorant and opacifying agent. It provides white or off-white color to tablets, capsules, and coatings while helping make formulations less transparent.
  • UNII 08MNR5YE2R
    A wax made in a laboratory to mimic natural beeswax. It's used as a coating, binder, and thickener to give medicines a smooth texture and protect them from moisture.
  • UNII 15FIX9V2JP
    Titanium dioxide is a bright white mineral powder commonly used as a colorant and opacifying agent. It makes pills and tablets white or lighter in color and helps make coatings non-transparent.
  • UNII R0ZB2556P8
    Tocopherol is a form of vitamin E derived from plant oils. It acts as an antioxidant in medicines to prevent oils and fats from breaking down and spoiling during storage.

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

The official label also statesPolybutene, Bis-Diglyceryl Polyacyladipate-2, Glycerin, Octyldodecanol, Synthetic Beeswax, Diisocetyl Dodecanedioate, Ricinus Communis (Castor) Seed Oil, Behenyl Alcohol, Polyglyceryl-3 Stearate, Carthamus Tinctorius (Safflower) Seed Oil, Silica Silylate, Fragrance, Menthol, Spirulina Maxima Extract, Laminaria Saccharina, Extract, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Saccharin, Aloe Barbadensis Leaf Extract, chamomilla recutita (matricaria) flower extract, Cucumis Sativus (Cucumber) Fruit Extract, Ascorbyl Palmitate, Tocopherol, Glycine Soja (Soybean) Oil, Iron Oxides, Red 7 Lake, Blue 1 Lake Polybutene, Bis-Diglyceryl Polyacyladipate-2, Glycerin, Octyldodecanol, Synthetic Beeswax, Diisocetyl Dodecanedioate, Ricinus Communis (Castor) Seed Oil, Behenyl Alcohol, Polyglyceryl-3 Stearate, Carthamus Tinctorius (Safflower) Seed Oil, Silica Silylate, Fragrance, Menthol, Spirulina Maxima Extract, Laminaria Saccharina, Extract, Saccharin, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Aloe Barbadensis Leaf Extract, chamomilla recutita (matricaria) flower extract, Cucumis Sativus (Cucumber) Fruit Extract, Ascorbyl Palmitate, Tocopherol, Glycine Soja (Soybean) Oil, Red 7 Lake, Blue 1 Lake Polybutene, Bis-Diglyceryl Polyacyladipate-2, Glycerin, Octyldodecanol, Synthetic Beeswax, Ricinus Communis (Castor) Seed Oil, Diisocetyl Dodecanedioate,, Behenyl Alcohol, Polyglyceryl-3 Stearate, Carthamus Tinctorius (Safflower) Seed Oil, Silica Silylate, Fragrance, Menthol, Laminaria Saccharina Extract, Spirulina Maxima Extract,, Saccharin, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate,, Aloe Barbadensis Leaf Extract, chamomilla recutita (matricaria) flower extract, Cucumis Sativus (Cucumber) Fruit Extract, Ascorbyl Palmitate, Tocopherol, Glycine Soja (Soybean) Oil, Red 7 Lake, Blue 1 Lake Polybutene, Bis-Diglyceryl Polyacyladipate-2, Glycerin, Octyldodecanol, Synthetic Beeswax, Diisocetyl Dodecanedioate, Ricinus Communis (Castor) Seed Oil, Behenyl Alcohol, Polyglyceryl-3 Stearate, Carthamus Tinctorius (Safflower) Seed Oil, Silica Silylate, Fragrance, Menthol, Laminaria Saccharina Extract, Spirulina Maxima Extract, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Saccharin, Aloe Barbadensis Leaf Extract, chamomilla recutita (matricaria) flower extract, Cucumis Sativus (Cucumber) Fruit Extract, Tin Oxide, Ascorbyl Palmitate, Tocopherol, Glycine Soja (Soybean) Oil, Mica, Titanium Dioxide, Iron Oxides, Red 7 Lake, Blue 1 Lake

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
Neutrogena MoistureShine Lip Soother with Sunscreen SPF 20, Glow 70 100 mg/g; 100 mg/g; 30 mg/gthis 69968-0852-01 Kenvue 10 g — — FDA listed —
Neutrogena MoistureShine Lip Soother with Sunscreen SPF 20, Gleam 40 100 mg/g; 100 mg/g; 30 mg/g 69968-0850-01 Kenvue 10 g — — FDA listed —
Neutrogena MoistureShine Lip Soother with Sunscreen SPF 20, Glaze 60 100 mg/g; 100 mg/g; 30 mg/g 69968-0851-01 Kenvue 10 g — — FDA listed —
Neutrogena MoistureShine Lip Soother with Sunscreen SPF 20, Shine 30 100 mg/g; 100 mg/g; 30 mg/g 69968-0849-01 Kenvue 10 g — — 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

🏛️
2024
On the market since
Apr 2024
📍
2026
Currently FDA-listed
2 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.

🔬 Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Avobenzone, Homosalate, Octocrylene — the ingredient across all brands.

Top reported reactions

Rash14
Erythema12
Headache12
Sunburn11
Acne10
Dry Skin10
Application Site Erythema9

Age at onset

Child1
Adult9
Elderly11

Reporter sex

180 reports
Male · 35%
Female · 65%

Serious outcomes

Hospitalization27
Death6
Disabling4
Life-threatening1
Reports over time (by year) — tap or hover for the count & year
2022 2023 2024 2026 12 3
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
69968-0852-01 You're viewing this 10 g in 1 TUBE (69968-0852-1) 2024-04-11 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 69968-0852-1, 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: 69968-0852-01, written without dashes as 69968085201. 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 69968-0852-01, the first segment (69968) is the labeler code FDA assigned to Kenvue Brands LLC; the middle segment (0852) 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 Kenvue Brands LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Kenvue Brands LLC 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 125 words ▾

Use • 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

Use • 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

Use • 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

Use • 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 ~2 min read ▾

Directions For Sunscreen Use • apply generously and evenly 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 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 of age: Ask a doctor

Directions For Sunscreen Use • apply generously and evenly 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 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 of age: Ask a doctor

Directions For Sunscreen Use • apply generously and evenly 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 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 of age: Ask a doctor

Directions For Sunscreen Use • apply generously and evenly 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 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 of age: Ask a doctor

⚠️ Warnings 216 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

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

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

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 68 words ▾

Other Information • protect this product from excessive heat and direct sun • may stain some fabrics

Other information • protect this product from excessive heat and direct sun • may stain some fabrics

Other information • protect this product from excessive heat and direct sun • may stain some fabrics

Other information • protect this product from excessive heat and direct sun • may stain some fabrics

🧪 Active Ingredient 32 words ▾

Active ingredient Avobenzone (3%), Homosalate (10%), Octocrylene (10%)

Active ingredients Avobenzone (3%), Homosalate (10%), Octocrylene (10%)

Active ingredients Avobenzone (3%), Homosalate (10%), Octocrylene (10%)

Active ingredients Avobenzone (3%), Homosalate (10%), Octocrylene (10%)

🧪 Inactive Ingredients ~1 min read ▾

Inactive ingredients Polybutene, Bis-Diglyceryl Polyacyladipate-2, Glycerin, Octyldodecanol, Synthetic Beeswax, Diisocetyl Dodecanedioate, Ricinus Communis (Castor) Seed Oil, Behenyl Alcohol, Polyglyceryl-3 Stearate, Carthamus Tinctorius (Safflower) Seed Oil, Silica Silylate, Fragrance, Menthol, Spirulina Maxima Extract, Laminaria Saccharina, Extract, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Saccharin, Aloe Barbadensis Leaf Extract, chamomilla recutita (matricaria) flower extract, Cucumis Sativus (Cucumber) Fruit Extract, Ascorbyl Palmitate, Tocopherol, Glycine Soja (Soybean) Oil, Iron Oxides, Red 7 Lake, Blue 1 Lake

Inactive ingredients Polybutene, Bis-Diglyceryl Polyacyladipate-2, Glycerin, Octyldodecanol, Synthetic Beeswax, Diisocetyl Dodecanedioate, Ricinus Communis (Castor) Seed Oil, Behenyl Alcohol, Polyglyceryl-3 Stearate, Carthamus Tinctorius (Safflower) Seed Oil, Silica Silylate, Fragrance, Menthol, Spirulina Maxima Extract, Laminaria Saccharina, Extract, Saccharin, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Aloe Barbadensis Leaf Extract, chamomilla recutita (matricaria) flower extract, Cucumis Sativus (Cucumber) Fruit Extract, Ascorbyl Palmitate, Tocopherol, Glycine Soja (Soybean) Oil, Red 7 Lake, Blue 1 Lake

Inactive ingredients Polybutene, Bis-Diglyceryl Polyacyladipate-2, Glycerin, Octyldodecanol, Synthetic Beeswax, Ricinus Communis (Castor) Seed Oil, Diisocetyl Dodecanedioate, , Behenyl Alcohol, Polyglyceryl-3 Stearate, Carthamus Tinctorius (Safflower) Seed Oil, Silica Silylate, Fragrance, Menthol, Laminaria Saccharina Extract, Spirulina Maxima Extract, , Saccharin , Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, , Aloe Barbadensis Leaf Extract, chamomilla recutita (matricaria) flower extract, Cucumis Sativus (Cucumber) Fruit Extract, Ascorbyl Palmitate, Tocopherol, Glycine Soja (Soybean) Oil, Red 7 Lake, Blue 1 Lake

Inactive ingredients Polybutene, Bis-Diglyceryl Polyacyladipate-2, Glycerin, Octyldodecanol, Synthetic Beeswax, Diisocetyl Dodecanedioate, Ricinus Communis (Castor) Seed Oil, Behenyl Alcohol, Polyglyceryl-3 Stearate, Carthamus Tinctorius (Safflower) Seed Oil, Silica Silylate, Fragrance, Menthol, Laminaria Saccharina Extract, Spirulina Maxima Extract, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Saccharin, Aloe Barbadensis Leaf Extract, chamomilla recutita (matricaria) flower extract, Cucumis Sativus (Cucumber) Fruit Extract, Tin Oxide, Ascorbyl Palmitate, Tocopherol, Glycine Soja (Soybean) Oil, Mica, Titanium Dioxide, Iron Oxides, Red 7 Lake, Blue 1 Lake

🎯 Purpose 8 words ▾

Purpose Sunscreen

Purpose Sunscreen

Purpose Sunscreen

Purpose Sunscreen

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.