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Pro-Collagen Marine Broad Spectrum SPF 30 AVOBENZONE, OCTINOXATE, and OCTOCRYLENE 10 mg/g; 10 mg/g; 5 mg/g Cream, 50 g — NDC 65912-0001-52 package photo

Pro-Collagen Marine Broad Spectrum SPF 30 AVOBENZONE, OCTINOXATE, and OCTOCRYLENE 10 mg/g; 10 mg/g; 5 mg/g Cream, 50 g

by ELEMIS Limited · 50 g in 1 JAR (65912-001-52)
NDC 65912-0001-52
🏷️ FDA NDC (as labeled) 65912-001-52 billing pads the product segment with a zero
This package
Contains50 g Pack sizes12 compare ↓
Also comes in: 100 g 65912-0001-10 15 g 65912-0001-15 30 g 65912-0001-30 50 g 65912-0001-50 15 g 65912-0001-18 2 jars 65912-0001-53 15 g 65912-0001-16 15 g 65912-0001-17 30 g 65912-0001-31 50 g 65912-0001-51 100 g 65912-0001-11
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) 65912-001-52
Product NDC 65912-001
11-digit billing NDC 65912000152
UNII G63QQF2NOX, 4Y5P7MUD51, 5A68WGF6WM
Application # M020
SPL Set ID 3321281e-612b-4305-bf6d-bfab02c65ffb
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2018-01-19
Route TOPICAL
Dosage form CREAM
Substance AVOBENZONE; OCTINOXATE; OCTOCRYLENE
Why two NDCs? The FDA registers this code as 65912-001-52 — 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 → 65912-0001-52. 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

LabelerELEMIS Limited
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code65912
First marketedJan 2018
Product typeHuman Otc Drug
Portfolio3 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?

Pro-Collagen Marine Broad Spectrum SPF 30 is a topical cream that functions as a sunscreen product. It contains three active ingredients: avobenzone, octinoxate, and octocrylene, which are ultraviolet (UV) light absorbers typically used together in sunscreen formulations to help protect skin from UV radiation. This is an over-the-counter monograph drug, meaning it is marketed under FDA's established rules for sunscreen products rather than as an individually reviewed 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.

💊 What it looks like

Color white
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

🧪 Inactive Ingredients / Excipients

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

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

  • UNII 9E8X80D2L0
    A synthetic form of vitamin E used as an antioxidant and preservative in medications. It helps prevent the active ingredients from degrading when exposed to oxygen or light.
  • UNII 8PHF3LSM61
    A natural gum extracted from Australian wattle flowers, used as a binder and thickening agent to help hold pill ingredients together and improve the medicine's texture and consistency.
  • 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 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 936JST6JCN
    Cetyl alcohol is a waxy, fatty substance derived from plant or animal sources. It acts as an emulsifier and thickener in medicines, helping blend oil and water components and giving products a smooth, creamy texture.
  • UNII RYQ4R60M02
    A green algae ingredient used as a natural colorant and nutritional filler in supplements and medications. It adds color and bulk to tablets and capsules.
  • UNII I670DAL4SZ
    A preservative that fights bacteria and fungi. It keeps medicines and topical products stable and safe from microbial contamination during storage and use.
  • 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 4828G836N6
    A plant-derived oil mixture from coconut that acts as an emollient and solvent. It helps dissolve or carry active ingredients and improves how the medicine spreads or absorbs in topical formulations.
  • UNII 609A3V1SUA
    A silky liquid derived from caprylic acid that acts as an emollient and solvent in formulations. It helps dissolve active ingredients and improves the spreadability and feel of lotions, creams, and topical products.
  • 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 19FUJ2C58T
    Ginkgo biloba leaf is a plant extract used as a flavoring or coloring agent in some medicines. It may also serve as a natural ingredient to support the product's formulation.
  • 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 FCZ5MH785I
    A waxy substance made from glycerin and stearic acid. It works as an emulsifier to help mix oil and water ingredients together, and as a thickener to give the medicine its proper texture and consistency.
  • 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 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 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 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 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 177U06NHZI
    A seaweed extract derived from the brown algae Padina pavonica. It's used as a moisturizing and skin-conditioning agent in topical formulations to help soften and hydrate the skin.
  • 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 5XB3A63Y52
    A synthetic rubber polymer used as a glidant and lubricant in tablet and capsule formulations. It reduces friction between particles and equipment surfaces, helping medicines flow smoothly during manufacturing and preventing sticking.
  • UNII 7T1F30V5YH
    A synthetic emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together and keeps them from separating in liquid formulations.
  • UNII K2P8K2558N
    A red marine microalga used as a natural colorant in medications and supplements. It provides red to purple coloring to tablets, capsules, and other formulations.
  • 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 CS4TE8FF7O
    A plant extract from the petals of the centifolia rose. It's used in medicines as a fragrance, flavoring agent, and for its pleasant scent and taste properties.
  • UNII K49155WL9Y
    Shea butter is a fat extracted from shea tree nuts. It's used in medicines as an emollient and lubricant to soften the product, improve texture, and help ingredients blend smoothly together.
  • 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 8W46YN971G
    Sodium dehydroacetate is a salt derived from dehydroacetic acid, a compound used as a preservative. It helps prevent mold, bacteria, and yeast growth in medicines, extending shelf life and maintaining product safety.
  • UNII 01S2G2C1E4
    Sorbitan isostearate is an emulsifier derived from sorbitol and isostearic acid. It helps mix oil and water-based ingredients together and keeps them blended throughout the medicine's shelf life.
  • UNII 4ELV7Z65AP
    Stearic acid is a fatty acid derived from plant or animal sources. It acts as a binder and lubricant in tablets and capsules, helping them hold together and flow smoothly during manufacturing.
  • UNII 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 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 14C97E680P
    Wheat germ oil is an oil extracted from wheat kernels. It's used in medicines as an emollient and lubricant to improve texture and help ingredients blend smoothly.
  • UNII 237DZG2JLA
    Whey protein hydrolysate is a milk-derived protein that has been broken down into smaller fragments. It serves as a binder and filler to help hold tablet or capsule ingredients together and add bulk to the formulation.
  • 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.

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

The official label also statesAQUA/WATER/EAU GLYCERIN CAPRYLIC/CAPRIC TRIGLYCERIDE GLYCERYL STEARATE SE ISONONYL ISONONANOATE DICAPRYLYL CARBONATE DIMETHICONE BUTYL METHOXYDIBENZOYLMETHANE ETHYLHEXYL METHOXYCINNAMATE PHENOXYETHANOL POLYACRYLATE-13 BUTYLENE GLYCOL CETYL ALCOHOL HYDROXYACETOPHENONE STEARIC ACID TOCOPHERYL ACETATE COCO-CAPRYLATE XANTHAN GUM CHLORPHENESIN POLYISOBUTENE FRAGRANCE (PARFUM) DISODIUM EDTA TOCOPHEROL BUTYROSPERMUM PARKII (SHEA) BUTTER TRITICUM VULGARE (WHEAT) GERM OIL CHLORELLA VULGARIS EXTRACT GLYCERYL POLYACRYLATE DAUCUS CAROTA SATIVA (CARROT) ROOT EXTRACT GLYCERYL ACRYLATE/ACRYLIC ACID COPOLYMER LECITHIN PADINA PAVONICA THALLUS EXTRACT SODIUM DEHYDROACETATE POLYSORBATE 20 SORBITAN ISOSTEARATE GINKGO BILOBA LEAF EXTRACT INGREDIENT NAME PORPHYRIDIUM CRUENTUM EXTRACT MIMOSA TENUIFLORA BARK EXTRACT ROSA DAMASCENA FLOWER EXTRACT COLLAGEN AMINO ACIDS LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE POTASSIUM SORBATE SODIUM BENZOATE CITRIC ACID

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: 100 g 15 g 30 g 50 g 15 g 2 jars 15 g 15 g 30 g 50 g 100 g
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
Pro-Collagen Marine Broad Spectrum SPF 30 10 mg/g; 10 mg/g; 5 mg/gthis 65912-0001-52 ELEMIS 50 g — — FDA listed —
Dynamic Resurfacing SPF 30 10 mg/g; 10 mg/g; 5 mg/g 65912-0002-50 ELEMIS 1 jar — — 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

🏛️
2018
On the market since
Jan 2018
📍
2026
Currently FDA-listed
8 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
65912-0001-10 1 JAR in 1 CARTON (65912-001-10) / 100 g in 1 JAR 2021-09-01 Active
65912-0001-11 100 g in 1 JAR (65912-001-11) 2021-09-01 Active
65912-0001-15 1 TUBE in 1 CARTON (65912-001-15) / 15 g in 1 TUBE 2018-01-19 Active
65912-0001-16 15 g in 1 TUBE (65912-001-16) 2018-01-19 Active
65912-0001-30 1 JAR in 1 CARTON (65912-001-30) / 30 g in 1 JAR 2020-07-31 Active
65912-0001-31 30 g in 1 JAR (65912-001-31) 2020-07-31 Active
65912-0001-50 1 JAR in 1 CARTON (65912-001-50) / 50 g in 1 JAR 2018-01-19 Active
65912-0001-51 50 g in 1 JAR (65912-001-51) 2018-01-19 Active
65912-0001-52 You're viewing this 50 g in 1 JAR (65912-001-52) 2018-01-19 Active
65912-0001-53 2 JAR in 1 CARTON (65912-001-53) / 50 g in 1 JAR 2019-09-01 Active
65912-0001-17 15 g in 1 JAR (65912-001-17) 2026-05-01 Active
65912-0001-18 1 JAR in 1 CARTON (65912-001-18) / 15 g in 1 JAR 2026-05-01 Active

Pack size FAQ

What quantity is in NDC 65912-0001-52?
NDC 65912-0001-52 contains 50 g — 50 g in 1 jar.
What is the difference between NDC 65912-0001-52 and NDC 65912-0001-16?
Both are Pro-Collagen Marine Broad Spectrum SPF 30 AVOBENZONE, OCTINOXATE, and OCTOCRYLENE 10 mg/g; 10 mg/g; 5 mg/g Cream — the drug itself is identical. NDC 65912-0001-52 is the 50 g package, while NDC 65912-0001-16 is the 15 g package.
What NDC number is used to bill for this package of Pro-Collagen Marine Broad Spectrum SPF 30 AVOBENZONE, OCTINOXATE, and OCTOCRYLENE 10 mg/g; 10 mg/g; 5 mg/g Cream?
Bill NDC 65912-0001-52 — the 11-digit billing format is 65912000152. 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 65912-001-52, 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: 65912-0001-52, written without dashes as 65912000152. 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 65912-0001-52, the first segment (65912) is the labeler code FDA assigned to ELEMIS Limited; the middle segment (0001) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (52) 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 ELEMIS Limited. 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 11 other package presentations of this same product, including 1 jar (65912-0001-10), 1 tube (65912-0001-15), 1 jar (65912-0001-30). 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?
ELEMIS Limited 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 10 words ▾

Uses helps prevent sunburn higher SPF gives more sunburn protection

⏱️ Dosage and Administration 98 words ▾

Directions apply liberally and evenly 15 minutes before sun exposure and as needed children under 6 months of age: Ask a doctor Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin ageing. 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 reapply at least every 2 hours use a water resistant sunscreen if swimming or sweating

⚠️ 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 9 words ▾

Active ingredients Avobenzone 1.0% } Octinoxate 1.0%} Octocrylene 0.5%}

🧪 Inactive Ingredients 104 words ▾

Inactive ingredients AQUA/WATER/EAU GLYCERIN CAPRYLIC/CAPRIC TRIGLYCERIDE GLYCERYL STEARATE SE ISONONYL ISONONANOATE DICAPRYLYL CARBONATE DIMETHICONE BUTYL METHOXYDIBENZOYLMETHANE ETHYLHEXYL METHOXYCINNAMATE PHENOXYETHANOL POLYACRYLATE-13 BUTYLENE GLYCOL CETYL ALCOHOL HYDROXYACETOPHENONE STEARIC ACID TOCOPHERYL ACETATE COCO-CAPRYLATE XANTHAN GUM CHLORPHENESIN POLYISOBUTENE FRAGRANCE (PARFUM) DISODIUM EDTA TOCOPHEROL BUTYROSPERMUM PARKII (SHEA) BUTTER TRITICUM VULGARE (WHEAT) GERM OIL CHLORELLA VULGARIS EXTRACT GLYCERYL POLYACRYLATE DAUCUS CAROTA SATIVA (CARROT) ROOT EXTRACT GLYCERYL ACRYLATE/ACRYLIC ACID COPOLYMER LECITHIN PADINA PAVONICA THALLUS EXTRACT SODIUM DEHYDROACETATE POLYSORBATE 20 SORBITAN ISOSTEARATE GINKGO BILOBA LEAF EXTRACT INGREDIENT NAME PORPHYRIDIUM CRUENTUM EXTRACT MIMOSA TENUIFLORA BARK EXTRACT ROSA DAMASCENA FLOWER EXTRACT COLLAGEN AMINO ACIDS LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE POTASSIUM SORBATE SODIUM BENZOATE CITRIC ACID

🎯 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 ↗
← 65898-0001-01 · Pulmonary 65912-0002-50 · ELEMIS →
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.