Home › NDC Lookup › Ingredients › Octocrylene, Homosalate, Octisalate, And... › 68479-0371-04
BIOLUMIN-C HEAT AGING PROTECTOR SPF50 Octocrylene, Homosalate, Octisalate, and Avobenzone 10 g/100mL; 7 g/100mL; 5 g/100mL; 3 g/100mL Lotion, 150 mL — NDC 68479-0371-04 package photo

BIOLUMIN-C HEAT AGING PROTECTOR SPF50 Octocrylene, Homosalate, Octisalate, and Avobenzone 10 g/100mL; 7 g/100mL; 5 g/100mL; 3 g/100mL Lotion, 150 mL

by Dermalogica, LLC. · 150 mL in 1 BOTTLE (68479-371-04)
NDC 68479-0371-04
🏷️ FDA NDC (as labeled) 68479-371-04 billing pads the product segment with a zero
This package
Contains150 mL Pack sizes4 compare ↓
Also comes in: 15 mL 68479-0371-01 50 mL 68479-0371-02 5 mL 68479-0371-05
OTC On market Non-controlled
🗂️ Data synced Aug 27, 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) 68479-371-04
Product NDC 68479-371
11-digit billing NDC 68479037104
UNII 5A68WGF6WM, V06SV4M95S, 4X49Y0596W, G63QQF2NOX
Application # M020
SPL Set ID 38d0b78b-bd8e-4cb0-925a-19adff550c19
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-05-22
Route TOPICAL
Dosage form LOTION
Substance OCTOCRYLENE; HOMOSALATE; OCTISALATE; AVOBENZONE
Why two NDCs? The FDA registers this code as 68479-371-04 — 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 → 68479-0371-04. 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

LabelerDermalogica, LLC.
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code68479
First marketedMay 2024
Product typeHuman Otc Drug
Portfolio17 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?

Biolumin-C Heat Aging Protector SPF50 is a topical lotion that contains multiple UV-filtering ingredients commonly used in sunscreen products. Octocrylene, homosalate, octisalate, and avobenzone function as ultraviolet (UV) absorbers, each working to help filter different wavelengths of sun exposure. This is an over-the-counter monograph product, meaning it is formulated according to FDA's established rules for sunscreen ingredients 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 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 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 290O2PQ83R
    A stabilized form of vitamin C used in topical products as an antioxidant ingredient. It helps prevent degradation of other active ingredients and maintains product stability during storage.
  • UNII M3PF9237YC
    A chemical compound made from vitamin C, combined with silicone and pectin, used as an antioxidant to prevent ingredients from breaking down and as a skin-conditioning agent in topical products.
  • UNII A3N5ZCN45C
    Bentonite is a naturally occurring clay mineral used in medicines as a binder and absorbent. It helps hold tablet ingredients together and can absorb moisture or unwanted substances in the formulation.
  • UNII 01YAE03M7J
    Beta carotene is a naturally occurring orange pigment found in plants. In medicines, it serves as a colorant to make tablets or capsules appear orange or yellow.
  • UNII 2U4T60A6YD
    Boron nitride is a synthetic mineral compound. It acts as a glidant and anti-caking agent to improve powder flow and prevent clumping in tablets and capsules.
  • 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 2EH13UN8D3
    A synthetic compound used as a solvent and penetration enhancer in topical formulations. It helps dissolve active ingredients and allows them to penetrate the skin more effectively.
  • UNII L56Z1JK48B
    A vegetable-derived ingredient used primarily as a natural colorant and flavoring agent in medicines. It provides orange-yellow color and mild taste to tablets, capsules, or liquids.
  • 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 2968PHW8QP
    A weak organic acid derived from citrus fruits or made through fermentation. It works as a buffer to control pH, a preservative to extend shelf life, and a flavoring agent in medications.
  • UNII F4K100DXP3
    Dibutyl adipate is a synthetic oily liquid derived from adipic acid. It serves as a plasticizer and solvent in medicines, helping softens coatings and improves flexibility so tablets and capsules don't crack or break.
  • UNII I0DQJ7YGXM
    A synthetic chemical compound used as a plasticizer in pharmaceutical coatings. It makes film coatings more flexible and durable so they don't crack or peel during manufacturing and storage.
  • UNII Q4R969U9FR
    A chelating agent derived from ethylenediamine, used in formulations to bind metal ions and prevent oxidation, helping preserve the medicine's stability and potency over time.
  • UNII WQ29KQ9POT
    Gluconolactone is a mild organic acid derived from glucose. It functions as a buffer and pH regulator in medicines, helping maintain stable acidity levels and improve product stability.
  • 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 YR377U58W9
    Grapefruit oil is a natural aromatic extract from grapefruit peel. It's used in medicines as a flavoring agent to improve taste and sometimes as a fragrance component.
  • UNII H1109Z9J4N
    A natural emulsifier derived from soybean oil. It helps mix oil and water-based ingredients together, ensuring even distribution of active ingredients throughout the medicine.
  • UNII G1L3HT4CMH
    A synthetic compound used in medicines as a preservative and antimicrobial agent. It helps prevent bacterial and fungal growth, extending the product's shelf life.
  • UNII 24WE03BX2T
    Levomenol is a naturally derived alcohol compound used as a skin-conditioning and anti-inflammatory agent in topical formulations. It helps soothe and protect the skin while improving product texture and absorption.
  • UNII 7937R189CB
    A natural oil extracted from Persian lime fruit, used as a flavoring agent to add citrus taste and aroma to medicines. It may also provide some antimicrobial properties in the formulation.
  • UNII GFD7C86Q1W
    A natural oil extracted from citrus peels, (+)-limonene is used as a flavoring agent and solvent in medicines. It helps dissolve active ingredients and provides a lemon or orange taste.
  • UNII NJO720F72R
    Mandarin oil is a natural essential oil extracted from mandarin orange peel. It's used as a flavor and aroma agent to make medicines taste and smell more pleasant.
  • UNII C9H2L21V7U
    A fat derived from coconut or palm oil containing shorter fatty acid chains. It serves as a solvent and carrier to help dissolve or suspend active ingredients, improving absorption and stability in liquid formulations.
  • UNII N8F53B3R4R
    A synthetic humectant and solvent derived from propane. It draws and holds moisture in the formulation, helping keep the medicine stable and improving texture or flow in liquid and semi-solid products.
  • UNII 5EVU04N5QU
    A natural or synthetic colorant that gives the medicine an orange hue. It helps identify the medication and may improve appearance.
  • UNII TI9T76XD44
    A natural flavoring derived from orange fruit peel. It adds orange taste and aroma to the medicine, making it more pleasant to take, while also providing natural color.
  • UNII GM2TDN9DZI
    A juice extract from physalis pubescens fruit, a plant in the nightshade family. It's used as a flavoring agent and natural coloring ingredient in medicines.
  • UNII 6OZP39ZG8H
    Polysorbate 80 is a synthetic emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together in medications and improves how the product disperses in the body.
  • 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 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 5965N8W85T
    Propanediol is a clear liquid organic compound derived from vegetable sources or synthesized chemically. It acts as a humectant to retain moisture, a solvent to dissolve active ingredients, and a preservative booster in liquid medications and supplements.
  • 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 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 55X04QC32I
    A strong alkaline chemical used to adjust and maintain the pH balance of liquid medicines. It helps keep the medicine stable and ensures it stays effective during storage.
  • UNII 65A9F4P024
    A synthetic compound derived from the amino acid glutamate and stearic acid. It acts as an emulsifier and surfactant to help mix oil and water-based ingredients, keeping the medicine uniform throughout.
  • UNII 1DI56QDM62
    A natural fatty substance from soybeans that helps mix oil and water-based ingredients together. It acts as an emulsifier and lubricant in medicines to improve texture and help the product break down properly in your body.
  • 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 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.
  • UNII YA22H34H9Q
    A chelating agent derived from sodium and organic compounds. It binds to metal ions in the formulation to improve stability and prevent unwanted chemical reactions that could degrade the medicine.
  • UNII C9TD27U172
    A plant-derived substance from mullein flowers, used as a natural flavoring agent or herbal additive in some formulations to provide taste or traditional botanical properties to the medicine.
  • UNII 035MV9S1C3
    A plastic-like polymer made from two chemical compounds joined together. It acts as a binder and film-former in tablets and capsules, helping hold ingredients together and create a protective coating on the medicine's surface.
  • 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 TTV12P4NEE
    Xanthan gum is a thickening and stabilizing ingredient made from fermented corn or other sugars. It's added to medicines to improve texture, prevent separation of liquids and solids, and help the product stay consistent.

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

The official label also statesWater/Aqua/Eau, Carthamus Tinctorius (Safflower) Oleosomes, Propanediol, Butyloctyl Salicylate, Bentonite, Butylene Glycol, Dibutyl Adipate, Polysorbate 80, Physalis Pubescens Fruit Juice, C12-15 Alkyl Benzoate, Diethylhexyl 2,6-Naphthalate, VP/Eicosene Copolymer, Aminopropyl Ascorbyl Phosphate, Hydroxyacetophenone, Dipotassium Glycyrrhizate, Glycine Soja (Soybean) Oil, Verbascum Thapsus Extract, Citrus Nobilis (Mandarin Orange) Peel Oil, Ricinus Communis (Castor) Seed Oil, Daucus Carota Sativa (Carrot) Root Extract, Citrus Aurantium Dulcis (Orange) Fruit Extract, Citrus Paradisi (Grapefruit) Fruit Extract, Glycerin, Citrus Aurantifolia (Lime) Oil, Tocopherol, Hydrogenated Lecithin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Allantoin, Ascorbyl Methylsilanol Pectinate, Beta-Carotene, Caprylic/Capric Triglyceride, Bisabolol, Gluconolactone, Lecithin, Boron Nitride, Xanthan Gum, Methylpropanediol, Silica, Sodium Stearoyl Glutamate, Potassium Cetyl Phosphate, Tetrahydroxypropyl Ethylenediamine, Trisodium Ethylenediamine Disuccinate, Citric Acid, Sodium Hydroxide, Sodium Acrylates Copolymer, Sodium Benzoate, Potassium Sorbate, Limonene, Citrus Species Peel Extract.

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.
Try another pack size: 15 mL 50 mL 5 mL
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
Biolumin-C Heat Aging Protector Spf50 10 g/100mL; 7 g/100mL; 5 g/100mL; 3 g/100mLthis 68479-0371-04 Dermalogica, 150 ml — — FDA listed —
Prisma Protect Spf30 10 g/100mL; 7 g/100mL; 5 g/100mL; 3 g/100mL 68479-0852-02 Dermalogica, 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

🏛️
2024
On the market since
May 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
68479-0371-01 1 BOTTLE in 1 CARTON (68479-371-01) / 15 mL in 1 BOTTLE 2024-05-22 Active
68479-0371-02 1 BOTTLE in 1 CARTON (68479-371-02) / 50 mL in 1 BOTTLE 2024-05-22 Active
68479-0371-04 You're viewing this 150 mL in 1 BOTTLE (68479-371-04) 2024-05-22 Active
68479-0371-05 1 BOTTLE in 1 CARTON (68479-371-05) / 5 mL in 1 BOTTLE 2024-05-22 Active

Pack size FAQ

What quantity is in NDC 68479-0371-04?
NDC 68479-0371-04 contains 150 mL — 150 ml in 1 bottle.
What NDC number is used to bill for this package of BIOLUMIN-C HEAT AGING PROTECTOR SPF50 Octocrylene, Homosalate, Octisalate, and Avobenzone 10 g/100mL; 7 g/100mL; 5 g/100mL; 3 g/100mL Lotion?
Bill NDC 68479-0371-04 — the 11-digit billing format is 68479037104. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 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 68479-371-04, 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: 68479-0371-04, written without dashes as 68479037104. 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 68479-0371-04, the first segment (68479) is the labeler code FDA assigned to Dermalogica, LLC.; the middle segment (0371) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (04) 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 Dermalogica, LLC.. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 3 other package presentations of this same product, including 1 bottle (68479-0371-01), 1 bottle (68479-0371-02), 1 bottle (68479-0371-05). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
Dermalogica, 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 31 words ▾

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

⏱️ Dosage and Administration 101 words ▾

Directions After cleansing and toning, apply generously to face 15 minutes prior to sun exposure. Reapply at least every two 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 help decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF 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-sleeve shirts, pants, hats and sunglasses Do not use on infants under 6 months old.

⚠️ 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 11 words ▾

Other information Protect this product from excessive heat and direct sun.

🧪 Active Ingredient 10 words ▾

Active Ingredients Avobenzone (3%) Homosalate (7%) Octisalate (5%) Octocrylene (10%)

🧪 Inactive Ingredients 124 words ▾

Inactive Ingredients Water/Aqua/Eau, Carthamus Tinctorius (Safflower) Oleosomes, Propanediol, Butyloctyl Salicylate, Bentonite, Butylene Glycol, Dibutyl Adipate, Polysorbate 80, Physalis Pubescens Fruit Juice, C12-15 Alkyl Benzoate, Diethylhexyl 2,6-Naphthalate, VP/Eicosene Copolymer, Aminopropyl Ascorbyl Phosphate, Hydroxyacetophenone, Dipotassium Glycyrrhizate, Glycine Soja (Soybean) Oil, Verbascum Thapsus Extract, Citrus Nobilis (Mandarin Orange) Peel Oil, Ricinus Communis (Castor) Seed Oil, Daucus Carota Sativa (Carrot) Root Extract, Citrus Aurantium Dulcis (Orange) Fruit Extract, Citrus Paradisi (Grapefruit) Fruit Extract, Glycerin, Citrus Aurantifolia (Lime) Oil, Tocopherol, Hydrogenated Lecithin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Allantoin, Ascorbyl Methylsilanol Pectinate, Beta-Carotene, Caprylic/Capric Triglyceride, Bisabolol, Gluconolactone, Lecithin, Boron Nitride, Xanthan Gum, Methylpropanediol, Silica, Sodium Stearoyl Glutamate, Potassium Cetyl Phosphate, Tetrahydroxypropyl Ethylenediamine, Trisodium Ethylenediamine Disuccinate, Citric Acid, Sodium Hydroxide, Sodium Acrylates Copolymer, Sodium Benzoate, Potassium Sorbate, Limonene, Citrus Species Peel Extract.

🎯 Purpose 2 words ▾

Purpose Sunscreen

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 68479-0350-00 · Dermalogica, 68479-0382-01 · Dermalogica, →
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.