Home › NDC Lookup › Ingredients › Avobenzone, Homosalate, Octisalate, Octy... › 84130-0011-13
Sunglaze Sheer Setting Mist Sunscreen SPF50 Avobenzone, Homosalate, Octisalate, Octyocrylene 5 mg/mL; 50 mg/mL; 100 mg/mL; 30 mg/mL Spray, 40 mL — NDC 84130-0011-13 package photo

Sunglaze Sheer Setting Mist Sunscreen SPF50 Avobenzone, Homosalate, Octisalate, Octyocrylene 5 mg/mL; 50 mg/mL; 100 mg/mL; 30 mg/mL Spray, 40 mL

by Koco Life LLC · 40 mL in 1 BOTTLE, PUMP (84130-011-13)
NDC 84130-0011-13
🏷️ FDA NDC (as labeled) 84130-011-13 billing pads the product segment with a zero
This package
Contains40 mL Pack sizes3 compare ↓
Also comes in: 2 bottles 84130-0011-93 75 ml 84130-0011-25
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) 84130-011-13
Product NDC 84130-011
11-digit billing NDC 84130001113
UNII V06SV4M95S, 4X49Y0596W, 5A68WGF6WM, G63QQF2NOX
UPC 0850077526602
Application # M020
SPL Set ID 22ce9b26-2bf8-c1ea-e063-6394a90a8ec2
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-09-23
Route TOPICAL
Dosage form SPRAY
Substance HOMOSALATE; OCTISALATE; OCTOCRYLENE; AVOBENZONE
Why two NDCs? The FDA registers this code as 84130-011-13 — 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 → 84130-0011-13. 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

LabelerKoco Life LLC
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code84130
First marketedSep 2024
Product typeHuman Otc Drug
Portfolio27 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

🩺 Clinical

🧪 What is this product?

This is a topical spray sunscreen marketed as an OTC monograph product. It contains four UV-filtering ingredients (avobenzone, homosalate, octisalate, and octocrylene) that are typically used together to help block ultraviolet radiation from the sun. The spray form allows application directly onto skin. Products of this type are commonly used to help reduce sun exposure.

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 7HLS05KP9O
    A natural flavoring compound derived from plants or created synthetically. It's added to medicines to improve taste by providing a creamy, fruity flavor note, making the medicine more pleasant to swallow.
  • UNII Z331YX9EL9
    A synthetic fragrance compound used as a flavoring agent in medicines. It provides taste and aroma to make oral medications more palatable, particularly in liquid formulations or chewable products.
  • UNII 3K9958V90M
    A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
  • UNII 9TLV70SV6I
    A natural essential oil extracted from bitter orange peel, used as a flavoring agent to mask unpleasant tastes and improve the palatability of medicines.
  • UNII 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 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 4X371TMK9K
    Dibutyl maleate is a synthetic chemical compound used as a plasticizer and solvent in pharmaceutical formulations. It helps soften and improve the flexibility of coatings and film-forming ingredients in medicines.
  • 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 P7E6YFV72X
    Diisopropyl adipate is a clear, oily liquid derived from adipic acid. It acts as a plasticizer and solvent in medicines, helping soften coatings and improve how the drug dissolves or spreads in the body.
  • UNII UFD2LZ005D
    Ethyl butyrate is a synthetic flavoring compound that smells fruity and buttery. It's added to medicines to improve taste and mask unpleasant flavors, making them easier to take.
  • UNII 1K09F3G675
    Ferric oxide red is an inorganic iron compound used as a colorant in medicines. It gives tablets, capsules, or other dosage forms a red or reddish tint for identification and appearance.
  • UNII L837108USY
    Geraniol is a natural fragrant compound found in plants like roses and lemons. It's used in medicines as a flavoring agent and to improve the taste or aroma of the product.
  • UNII 3W81YG7P9R
    Geranyl acetate is a fragrant compound derived from natural plant sources. It is used in medicines as a flavoring agent to improve taste or as a fragrance component.
  • 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 7U7KU3MWT0
    Hexyl acetate is a synthetic liquid compound used as a solvent and flavoring agent in medicines. It helps dissolve other ingredients and can contribute to the taste or aroma of the formulation.
  • UNII YSE9PPT4TH
    Hyaluronate sodium is a natural carbohydrate that holds moisture. It's used in medicines as a lubricant, thickener, and moisture-retaining agent to improve texture and delivery of the active ingredient.
  • UNII ZF94AP8MEY
    Hydrogenated castor oil is a processed plant oil made by adding hydrogen to castor oil. It's used as a binder to help hold tablet ingredients together and as a lubricant to prevent sticking during manufacturing.
  • UNII G5SU0BFK7O
    A synthetic compound made from lauryl alcohol and lactic acid. It works as an emulsifier and solubilizer to help mix oil and water-based ingredients and improve how the medicine dissolves or spreads.
  • UNII UZH29XGA8G
    Lime oil is a natural fragrant liquid extracted from lime fruit peel. It's used in medicines as a flavoring agent to mask bitter or unpleasant tastes, making the medicine more pleasant to take.
  • 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 2XIW34BN6O
    A fragrant oil derived from litsea cubeba fruit, used as a flavoring agent and aromatic ingredient to improve the taste and smell of the medicine.
  • UNII 3A9RD92BS4
    Maltol is a naturally occurring organic compound found in foods like bread crust and coffee. In medicines, it acts as a flavoring agent to mask bitter tastes and improve palatability.
  • UNII V8A1AW0880
    Mica is a naturally occurring mineral that's ground into fine powder. It's used in medicines as a colorant and anti-caking agent to improve appearance and prevent clumping in tablets or powders.
  • UNII AKN3KSD11B
    Orange oil obtained by cold pressing orange peel. It serves as a flavoring agent and fragrance in medicines to improve taste and aroma.
  • UNII 788QAG3W8A
    A synthetic polymer that combines polyethylene glycol, glycidyl ether, and sodium hyaluronate. It acts as a thickener and film-former in topical products, helping maintain texture and improve how the medicine spreads on skin.
  • UNII MGE3733FR2
    Polyglutamic acid is a synthetic polymer made from linked amino acids. In medications, it acts as a binder to hold tablet ingredients together and may help control how quickly the drug dissolves and releases in your body.
  • 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 R60QEP13IC
    Rice bran is a natural powder made from the outer layer of rice grains. It's used in medicines as a filler and flow agent to add bulk and help the product mix and flow smoothly during manufacturing.
  • 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 C3M81465G5
    Spearmint oil is a natural flavoring extract from spearmint plants. It's added to medicines to improve taste and mask bitter flavors, making medications easier to take.
  • UNII JB2MV9I3LS
    Stannous oxide is a tin-based compound used as a polishing agent in toothpaste formulations. It helps remove surface stains and create a smooth tooth surface during brushing.
  • UNII R53Q4ZWC99
    Terpineol is a fragrant alcohol derived from pine oil or other plant sources. It's used in medicines as a flavoring agent and to improve the taste or aroma of the product.
  • UNII MD83SFE959
    A volatile organic liquid used as a solvent and preservative in medications. It helps dissolve active ingredients and other components, and can improve product stability and shelf life.
  • UNII 9LBV3F07AZ
    A synthetic, oil-soluble form of vitamin C used as an antioxidant to prevent degradation of the medicine and maintain its stability during storage.
  • 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.
  • UNII 8Z96QXD6UM
    Triethyl citrate is a clear liquid derived from citric acid. It acts as a plasticizer and solvent in tablet coatings and film formulations, helping the coating remain flexible and adhere properly to the medicine.
  • 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.

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

The official label also statesAlcohol Denat., Butyloctyl Salicylate, Diisopropyl Adipate, Lauryl Lactate, Dicaprylyl Carbonate, Sodium Hyaluronate, Sodium Hyaluronate Crosspolymer, Tetrahexyldecyl Ascorbate, Tocopherol, Citrus Aurantifolia (Lime) Oil, Litsea Cubeba Fruit Oil, Citrus Aurantium Dulcis (Orange) Peel Oil, Mentha Viridis (Spearmint) Leaf Oil, Citrus Aurantium Peel Oil, Hydrogenated Castor Oil, Oryza Sativa (Rice) Bran Extract, Communis (Castor) Seed Oil, Glycerin, Triethyl Citrate, Gamma Decalactone, Maltol, Dimethyl Heptenal, Hexyl Acetate, Ethyl Butyrate, VA/Butyl Maleate/Isobornyl Acrylate Copolymer, t-Butyl Alcohol, Mica, Water/Aqua/Eau, Propanediol, Polyglutamic Acid, Citric Acid, Sodium Benzoate, Limonene, Geraniol, Geranyl Acetate, Terpineol, 3,6-Nonadienol, Tin Oxide, CI 77891 (Titanium DIoxide), CI 77491 (Iron Oxides).

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.
Try another pack size: 2 bottles 75 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
Sunglaze Sheer Setting Mist Sunscreen SPF50 5 mg/mL; 50 mg/mL; 100 mg/mL; 30 mg/mLthis 84130-0011-13 Koco 40 ml — — 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
Sep 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
84130-0011-13 You're viewing this 40 mL in 1 BOTTLE, PUMP (84130-011-13) 2024-09-23 Active
84130-0011-25 75 mL in 1 BOTTLE, PUMP (84130-011-25) 2024-09-23 Active
84130-0011-93 2 BOTTLE, PUMP in 1 CARTON (84130-011-93) / 75 mL in 1 BOTTLE, PUMP 2026-01-15 Active

Pack size FAQ

What quantity is in NDC 84130-0011-13?
NDC 84130-0011-13 contains 40 mL — 40 ml in 1 bottle, pump.
What is the difference between NDC 84130-0011-13 and NDC 84130-0011-25?
Both are Sunglaze Sheer Setting Mist Sunscreen SPF50 Avobenzone, Homosalate, Octisalate, Octyocrylene 5 mg/mL; 50 mg/mL; 100 mg/mL; 30 mg/mL Spray — the drug itself is identical. NDC 84130-0011-13 is the 40 mL package, while NDC 84130-0011-25 is the 75 ml package.
What NDC number is used to bill for this package of Sunglaze Sheer Setting Mist Sunscreen SPF50 Avobenzone, Homosalate, Octisalate, Octyocrylene 5 mg/mL; 50 mg/mL; 100 mg/mL; 30 mg/mL Spray?
Bill NDC 84130-0011-13 — the 11-digit billing format is 84130001113. 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 84130-011-13, 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: 84130-0011-13, written without dashes as 84130001113. 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 84130-0011-13, the first segment (84130) is the labeler code FDA assigned to Koco Life LLC; the middle segment (0011) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (13) 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 Koco Life 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 2 other package presentations of this same product, including 2 bottles (84130-0011-93), 75 ml (84130-0011-25). 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?
Koco Life 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 30 words ▾

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

⏱️ Dosage and Administration 117 words ▾

Directions Shake well before use. With eyes closed, spray generously and evenlyover your face while holding spray 8-10 inches away. Apply 15 minutesbefore sun exposure. • Reapply: After 40 minutes of swimming orsweating. • Immediately after towel drying. • At least every 2 hours.

Do notspray directly into eyes • Sun Protection Measures Spending time in thesun increases your risk of skin cancer & early skin aging. To decrease thisrisk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 orhigher & other sun protection measures including: • Limit time in the sun,especially from 10 a.m. - 2 p.m. • Wear long-sleeved shirts, hats, andsunglasses • Children under 6 months of age: Ask a doctor

⚠️ Warnings 61 words ▾

Warnings For external use only ● Do not use on damage or broken skin ● When using this product keep out of eyes. Rinse with water to remove. ● Stop use and ask a doctor if a rash occurs. ● Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

📦 Storage and Handling 16 words ▾

Other Information • Protect this product fromexcessive heat and direct sun • May stain some fabrics

🧪 Active Ingredient 10 words ▾

Active ingredients Avobenzone 3%, Homosalate 0.5%, Octisalate 5%, Octyocrylene 10%

🧪 Inactive Ingredients 98 words ▾

Inactive Ingredients Alcohol Denat., Butyloctyl Salicylate, Diisopropyl Adipate, Lauryl Lactate, Dicaprylyl Carbonate, Sodium Hyaluronate, Sodium Hyaluronate Crosspolymer, Tetrahexyldecyl Ascorbate, Tocopherol, Citrus Aurantifolia (Lime) Oil, Litsea Cubeba Fruit Oil, Citrus Aurantium Dulcis (Orange) Peel Oil, Mentha Viridis (Spearmint) Leaf Oil, Citrus Aurantium Peel Oil, Hydrogenated Castor Oil, Oryza Sativa (Rice) Bran Extract, Communis (Castor) Seed Oil, Glycerin, Triethyl Citrate, Gamma Decalactone, Maltol, Dimethyl Heptenal, Hexyl Acetate, Ethyl Butyrate, VA/Butyl Maleate/Isobornyl Acrylate Copolymer, t-Butyl Alcohol, Mica, Water/Aqua/Eau, Propanediol, Polyglutamic Acid, Citric Acid, Sodium Benzoate, Limonene, Geraniol, Geranyl Acetate, Terpineol, 3,6-Nonadienol, Tin Oxide, CI 77891 (Titanium DIoxide), CI 77491 (Iron Oxides).

🎯 Purpose 9 words ▾

Purpose Avobenzone 3%, Homosalate 0.5%, Octisalate 5%, Octyocrylene 10%.................Sunscreen

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 84130-0010-07 · Koco 84130-0012-50 · Koco →
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.