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CERAMIDE LIFT and FIRM EYE SPF 15 Oxybenzone, Octinoxate 4.1 mg/g; 1.4 mg/g Emulsion, 14.4 g

by REVLON · 14.4 g in 1 JAR (10967-667-61)
NDC 10967-0667-61
🏷️ FDA NDC (as labeled) 10967-667-61 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) 10967-667-61
Product NDC 10967-667
11-digit billing NDC 10967066761
UNII 4Y5P7MUD51, 95OOS7VE0Y
Application # M020
SPL Set ID b22f0c13-0a9c-7d38-e053-2a95a90a0ecd
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2019-04-19
Route TOPICAL
Dosage form EMULSION
Substance OCTINOXATE; OXYBENZONE
Why two NDCs? The FDA registers this code as 10967-667-61 — 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 → 10967-0667-61. 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

LabelerREVLON
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code10967
First marketedApr 2019
Product typeHuman Otc Drug
Portfolio18 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 an over-the-counter eye cream emulsion applied to the skin around the eyes. It contains two UV-filtering ingredients, octinoxate and oxybenzone, which are commonly used in sunscreen products to help absorb and block ultraviolet light from the sun. The product is marketed under FDA's monograph rules for sunscreen drugs rather than as an individually approved application. The formulation also includes ceramides, which are lipid compounds typically found in moisturizing products.

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 UN2QZ55I88
    A plant-derived ingredient from abelmoschus moschatus seeds. It's used in formulations as a thickening agent, emulsifier, and texture enhancer to help bind and stabilize medicine ingredients.
  • UNII 8K14HJF88S
    A synthetic peptide made of eight amino acids linked together. It's used in some formulations as a conditioning or skin-feel agent to help improve product texture and appearance on the skin.
  • 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 W59H9296ZG
    A synthetic polymer made from acrylic compounds and vinylpyrrolidone. It works as a film-former and thickener in topical products, helping create a smooth texture and improve how the medication spreads on skin.
  • 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 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 2CNS542YRT
    A silicone-based compound that acts as an emulsifier and surfactant to help blend oil and water ingredients together. It improves the texture and spreadability of topical products like creams and lotions.
  • UNII 1P9D0Z171K
    BHT is a synthetic antioxidant that prevents fats and oils in medicines from breaking down and becoming rancid. It helps keep the product stable and effective during storage.
  • 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 R12CBM0EIZ
    A natural wax derived from a Brazilian palm tree, used as a coating and polish on tablets and capsules. It creates a smooth, shiny finish that protects the medicine and improves appearance.
  • UNII 4370DF050B
    Ceramide NP is a waxy, lipid-based substance that mimics natural skin oils. It's used in topical formulations as an emollient and skin-conditioning agent to help soften, smooth, and protect the skin barrier.
  • UNII I835H2IHHX
    A waxy substance derived from plant oils, used as an emulsifier and solubilizer to help mix oil and water ingredients together and keep them blended throughout the product's shelf life.
  • UNII 2DMT128M1S
    A waxy solid derived from plant or animal sources. It acts as an emulsifier to blend oil and water components, and also thickens the medicine to give it the right texture and consistency.
  • UNII 1P677500YD
    Cetyl ricinoleate is a waxy substance derived from castor oil. It works as an emollient and thickener in medications, helping to soften the product and improve its texture and stability.
  • UNII MOR84MUD8E
    Chlorhexidine digluconate is an antimicrobial compound added to some medicines as a preservative to prevent bacterial and fungal growth, extending shelf life and maintaining product safety.
  • UNII 97C5T2UQ7J
    Cholesterol is a fatty substance found naturally in animal tissues. In medications, it's used as an ingredient in liposomal formulations and lipid-based drug delivery systems to help encapsulate and stabilize active drugs for better absorption.
  • 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 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 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 W2ZU1RY8B0
    A plant extract from green tea leaves. It's used as an antioxidant ingredient to help preserve the medicine and maintain its stability during storage.
  • UNII KEH0A3F75J
    Hexylene glycol is a clear liquid alcohol used as a solvent and preservative in medicines. It helps dissolve other ingredients and keeps the product stable during storage.
  • UNII 7D1YQ9Y5EZ
    Hydrogenated polybutene is a thick, wax-like ingredient made by chemically processing petroleum. It acts as a binder and lubricant, helping hold tablet ingredients together and allowing pills to slide smoothly during manufacturing and packaging.
  • UNII S4V5BS6GCX
    A synthetic oily liquid used as an emollient and solvent in topical medications. It helps dissolve active ingredients and creates a smooth, spreadable texture on the skin.
  • UNII D2QHA03458
    A fermented ingredient made by culturing beneficial bacteria in radish root extract. It acts as a natural preservative and humectant, helping keep the product fresh and maintain moisture in the formula.
  • UNII 58U0NZN2BT
    Myristyl laurate is a waxy ester made from natural fatty acids. It functions as a lubricant and binder in tablets and capsules to improve how they flow during manufacturing and help hold ingredients together.
  • UNII 4042ZC00DY
    A waxy ester derived from myristic acid, used as an emollient and lubricant in topical formulations. It helps soften skin contact, reduce friction during application, and improve the texture and spreadability of creams and ointments.
  • UNII Q41S464P1R
    A synthetic peptide (short protein-like molecule) used in skincare and cosmetic formulations as an active conditioning ingredient to help improve skin texture and appearance. It may function as a humectant or skin-conditioning agent in topical products.
  • UNII YD01N1999R
    A waxy substance made from polyethylene glycol and stearic acid. It helps mix oil and water-based ingredients together and serves as an emulsifier and solubilizer in liquid and semi-solid medicines.
  • UNII 50C1307PZG
    Pentylene glycol is a humectant and preservative helper derived from petroleum or plant sources. It draws moisture into the product and helps prevent bacterial growth, keeping medicines stable 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 GIN46U9Q2Q
    Phytosphingosine is a naturally derived fatty compound that helps stabilize and thicken skincare and cosmetic formulations. It works as an emollient and conditioning agent to improve texture and skin feel in topical products.
  • UNII U076Q6Q621
    Polyethylene glycol 1000 is a synthetic compound made from ethylene oxide. It serves as a solvent, lubricant, and humectant in medicines, helping dissolve active ingredients and improve how the product flows and feels.
  • 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 FZ989GH94E
    Povidone is a synthetic polymer made from a plastic-like material. It acts as a binder to hold tablet ingredients together and as a disintegrant to help the tablet break apart in your stomach so the medicine can be absorbed.
  • UNII BI6C7YO419
    A synthetic oily liquid derived from petroleum-based materials. It functions as an emulsifier and solubilizer in medicines, helping blend water and oil-based ingredients and keeping them mixed throughout the product's 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 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 7243K85WFO
    Sodium lauroyl lactylate is a mild surfactant derived from natural fats and lactic acid. It acts as an emulsifier and solubilizer to help blend oil and water-based ingredients and improve how the body absorbs the active drug.
  • UNII 6LUM696811
    A waxy substance derived from sorbitol and stearic acid. It acts as an emulsifier and stabilizer to help mix oil and water components evenly throughout the medicine and prevent separation.
  • UNII L7HT8F1ZOD
    A plant-based oil extracted from soybeans. It's used as an emulsifier and lubricant to help mix ingredients evenly and prevent sticking during tablet or capsule manufacturing.
  • UNII 4OH5W9UM87
    A synthetic emulsifier and surfactant derived from stearic acid. It helps oils and water mix together in liquid medicines and creams, and improves how the product spreads and feels on the skin.
  • UNII L0Q8IK9E08
    A synthetic compound made from stearic acid and polyethylene glycol. It acts as an emulsifier and solubilizer, helping mix oil and water-based ingredients and keeping them blended throughout the medicine's shelf life.
  • UNII 2M4UGL1NCN
    Stearyl heptanoate is a waxy ester made by combining stearyl alcohol and heptanoic acid. It's used in medicines as a lubricant and thickening agent to improve texture and help the product flow smoothly during manufacturing.
  • 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 9O3K93S3TK
    Trolamine is an alkaline compound used as a pH buffer and emulsifier in medicines. It helps neutralize acids, stabilize formulations, and enable mixing of oil and water-based ingredients.
  • UNII 3G64B4AFQN
    A dipeptide is a small protein fragment made of two amino acids joined together. In medications, it may serve as a humectant to retain moisture, a skin-conditioning agent, or a stabilizer to help maintain product quality.
  • 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.

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

The official label also statesOther Ingredients: Aqua/Water/Eau, Dimethicone, Cetyl Ricinoleate, Cetearyl Alcohol, Glycerin, Synthetic Beeswax, Butylene Glycol, Pentylene Glycol, Stearyl Heptanoate, Hydrogenated Polyisobutene, Myristyl Myristate, Isononyl Isononanoate, Cetearyl Dimethicone Crosspolymer, Ammonium Acryloyldimethyltaurate/VP Copolymer, Cera Carnauba/Copernicia Cerifera (Carnauba) Wax/Cire de carnauba, PPG-2 Isoceteth-20 Acetate, Acetyl Octapeptide-3, Ascorbyl Glucoside, Ascorbyl Palmitate, Bis-PEG-12 Dimethicone, Camellia Sinensis Leaf Extract, Caprylyl Glycol, Cera Alba/Beeswax/Cire D'abeille, Ceramide AP, Ceramide EOP, Ceramide NP, Ceteth-20, Cholesterol, Cyclopentasiloxane, Dipeptide-2, Disodium EDTA, Glycine Soja (Soybean) Seed Extract, Hexylene Glycol, Hibiscus Abelmoschus Seed Extract, Leuconostoc/Radish Root Ferment Filtrate, Myristyl Laurate, Palmitoyl Tetrapeptide-7, PEG-100 Stearate, PEG-20, Phospholipids, Phytosphingosine, PVP, Pyrus Malus (Apple) Fruit Extract, Silica, Sodium Hydroxide, Sodium Lauroyl Lactylate, Sorbitan Tristearate, Steareth-100, Steareth-20, Tocopheryl Acetate, Triethanolamine, VP/Eicosene Copolymer, Xanthan Gum, BHT, Hesperidin Methyl Chalcone, Chlorhexidine Digluconate, Phenoxyethanol, Potassium Sorbate.

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 mLPer 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
CERAMIDE LIFT and FIRM EYE SPF 15 4.1 mg/g; 1.4 mg/gthis 10967-0667-61 REVLON 14.4 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

🏛️
2019
On the market since
Apr 2019
📍
2026
Currently FDA-listed
7 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
10967-0667-61 You're viewing this 14.4 g in 1 JAR (10967-667-61) 2019-04-19 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 10967-667-61, 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: 10967-0667-61, written without dashes as 10967066761. 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 10967-0667-61, the first segment (10967) is the labeler code FDA assigned to REVLON; the middle segment (0667) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (61) 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 REVLON. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
REVLON 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 3 words ▾

Helps prevent sunburn

⏱️ Dosage and Administration 2 words ▾

As needed

⚠️ Warnings 97 words ▾

WARNINGS Warnings Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to prevent sunburn, not skin cancer or early skin aging. - 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 product is swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 14 words ▾

ACTIVE INGREDIENTS PURPOSE Active Ingredients Purpose OCTINOXATE 4.1% ....... Sunscreen OXYBENZONE 1.4% ....... Sunscreen

🧪 Inactive Ingredients 126 words ▾

OTHER INGREDIENTS Other Ingredients: Aqua/Water/Eau, Dimethicone, Cetyl Ricinoleate, Cetearyl Alcohol, Glycerin, Synthetic Beeswax, Butylene Glycol, Pentylene Glycol, Stearyl Heptanoate, Hydrogenated Polyisobutene, Myristyl Myristate, Isononyl Isononanoate, Cetearyl Dimethicone Crosspolymer, Ammonium Acryloyldimethyltaurate/VP Copolymer, Cera Carnauba/Copernicia Cerifera (Carnauba) Wax/Cire de carnauba, PPG-2 Isoceteth-20 Acetate, Acetyl Octapeptide-3, Ascorbyl Glucoside, Ascorbyl Palmitate, Bis-PEG-12 Dimethicone, Camellia Sinensis Leaf Extract, Caprylyl Glycol, Cera Alba/Beeswax/Cire D'abeille, Ceramide AP, Ceramide EOP, Ceramide NP, Ceteth-20, Cholesterol, Cyclopentasiloxane, Dipeptide-2, Disodium EDTA, Glycine Soja (Soybean) Seed Extract, Hexylene Glycol, Hibiscus Abelmoschus Seed Extract, Leuconostoc/Radish Root Ferment Filtrate, Myristyl Laurate, Palmitoyl Tetrapeptide-7, PEG-100 Stearate, PEG-20, Phospholipids, Phytosphingosine, PVP, Pyrus Malus (Apple) Fruit Extract, Silica, Sodium Hydroxide, Sodium Lauroyl Lactylate, Sorbitan Tristearate, Steareth-100, Steareth-20, Tocopheryl Acetate, Triethanolamine, VP/Eicosene Copolymer, Xanthan Gum, BHT, Hesperidin Methyl Chalcone, Chlorhexidine Digluconate, Phenoxyethanol, Potassium Sorbate.

🎯 Purpose 1 words ▾

Sunscreen

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 10967-0666-17 · REVLON 10967-0668-01 · REVLON →
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.