Home › NDC Lookup › Ingredients › Homosalate, Octisalate, Octocrylene, Zin... › 60232-1022-00
🧴image loading
(from DailyMed)

Image Skincare Prevention Plus Daily Ultimate Protection homosalate, octisalate, octocrylene, zinc oxide sunscreen 100 g/1000g; 50 g/1000g; 60 g/1000g; 90 g/1000g Cream, 7 g

by Swiss-American CDMO, LLC · 7 g in 1 TUBE (60232-1022-0)
NDC 60232-1022-00
🏷️ FDA NDC (as labeled) 60232-1022-0 billing pads the package segment with a zero
This package
Contains7 g Pack sizes2 compare ↓
Also comes in: 91 g 60232-1022-03
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) 60232-1022-0
Product NDC 60232-1022
11-digit billing NDC 60232102200
UNII V06SV4M95S, 4X49Y0596W, 5A68WGF6WM, SOI2LOH54Z
Application # M020
SPL Set ID 3473f94c-5faf-4415-9605-f58ec93cd268
Established class (EPC) Copper Absorption Inhibitor
Physiologic effect Decreased Copper Ion Absorption
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2020-01-31
Route TOPICAL
Dosage form CREAM
Substance HOMOSALATE; OCTISALATE; OCTOCRYLENE; ZINC OXIDE
Why two NDCs? The FDA registers this code as 60232-1022-0 — a 5-4-1 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the package segment → 60232-1022-00. 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

LabelerSwiss-American CDMO, LLC
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code60232
First marketedJan 2020
Product typeHuman Otc Drug
Portfolio15 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 sunscreen cream applied to the skin. It contains four active ingredients that function as ultraviolet light filters: homosalate, octisalate, and octocrylene are organic UV absorbers, while zinc oxide is a mineral reflectant. These ingredients are typically combined in sunscreen products to help protect exposed skin from UV radiation. As an OTC monograph drug, this product is marketed under FDA's established rules for sunscreen formulations 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 JU84X1II0N
    Delta-tocopherol is a form of vitamin E, a fat-soluble antioxidant. It's used in medicines as a preservative to prevent oils and fats from breaking down and spoiling.
  • UNII KOS935A04V
    A fragrant oil extracted from buchu leaves (Agathosma betulina), a plant native to South Africa. Used in medicines as a flavor enhancer and fragrance component to improve taste and aroma.
  • UNII XF417D3PSL
    Anhydrous citric acid is a sour, crystalline powder derived from citric acid with water removed. In medicines, it acts as a buffer to control pH, adds tartness to improve taste, and helps tablets disintegrate.
  • UNII AI3L60HQ81
    A plant-derived substance from the model plant Arabidopsis thaliana, used as a natural binder or thickening agent to help hold the medicine together and improve its texture and stability.
  • UNII 9M64UO4C25
    A synthetic oily substance used as an emollient and texture enhancer in medicines. It helps soften formulations, improves how the medicine spreads or feels on skin, and can act as a lubricant in tablets or capsules.
  • UNII V2W71V8T0X
    A silicone-based compound that mixes oil and water together. Used in formulations as an emulsifier to help blend ingredients and improve texture and stability of creams, lotions, and other topical products.
  • 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 X687XDK09L
    A clay mineral processed to carry positive charges, used as a thickener and suspending agent in liquid medicines. It helps keep solid particles evenly distributed throughout the product.
  • UNII 7FLD91C86K
    Edetate disodium is a chemical compound that binds and removes certain metal ions. In medicines, it acts as a preservative and stabilizer by preventing metals like calcium from interfering with the product's shelf life and consistency.
  • UNII BDZ3DQM98W
    Ergothioneine is a naturally occurring compound found in mushrooms and some bacteria. It's used in medicines as an antioxidant to help protect the product from degradation during storage.
  • UNII RA96B954X6
    Erythritol is a sugar alcohol derived from fermented fruits or grains. It's used as a sweetener and bulking agent in medicines to improve taste without adding significant calories.
  • UNII 147D247K3P
    Ethylhexylglycerin is a synthetic preservative used to prevent bacteria and mold from growing in medicines and personal care products. It helps keep the product safe and stable throughout its shelf life.
  • 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 8866LNG61N
    Homarine hydrochloride is a naturally occurring compound derived from marine organisms. In medicines, it functions as a buffer and pH regulator to maintain the correct acidity level in liquid formulations.
  • UNII S270N0TRQY
    Hyaluronic acid is a naturally occurring substance found in skin and joints. In medicines, it acts as a moisturizer and thickening agent to improve texture and help the product spread smoothly.
  • UNII X33R8U0062
    Isostearic acid is a fatty acid derived from vegetable oils. It acts as an emulsifier and lubricant in medicines, helping blend ingredients together and reducing friction during tablet or capsule manufacturing.
  • 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 9MC3I34447
    A natural oil extracted from citrus peel, used as a flavoring agent and solvent to improve taste and help dissolve or distribute other ingredients in the medicine.
  • UNII 04W636S1V3
    A powdered ingredient made from dried whole apple fruit. It adds bulk to the tablet or capsule and may help bind ingredients together while contributing natural flavor and fiber.
  • UNII 7A72MUN24Z
    Marrubium vulgare, also called horehound, is a plant extract used as a flavoring and soothing agent in cough drops and lozenges. It provides taste and traditional herbal characteristics to the medicine.
  • 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 LV6L29Z6AX
    A naturally occurring bacterium used as a preservative in some medications and cosmetics. It helps prevent microbial growth and extends product shelf life.
  • 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 WV9CM0O67Z
    Panthenol is a humectant and skin-conditioning agent derived from pantothenic acid. It's added to medicines to help retain moisture and soothe skin irritation.
  • UNII CCX72L6NY6
    A synthetic plastic polymer made from polyethylene glycol and a cross-linking agent. It acts as a film-former and binder in medications, helping create smooth coatings on tablets or holding ingredients together in solid dosage forms.
  • 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 7B8OE71MQC
    A synthetic emulsifier derived from glycerin and fatty acids. It helps oils and water mix together in formulations, keeping ingredients evenly distributed throughout the product.
  • UNII YXH47AOU0F
    A synthetic fatty acid used as a thickener and stabilizer in medicines. It helps create the right texture and prevents separation of ingredients in liquid or semi-solid formulations.
  • 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 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 451W47IQ8X
    Sodium chloride is common table salt. It's used in medicines as a buffer to maintain proper pH, as a filler to add bulk, or to adjust the osmotic balance in liquid formulations.
  • UNII V8ZGC8ISR3
    Sodium succinate anhydrous is a salt derived from succinic acid. It acts as a buffer to help maintain the medicine's pH and may also serve as a filler to give the tablet or capsule proper volume and texture.
  • UNII 3W1JG795YI
    Sunflower oil is a natural vegetable oil derived from sunflower seeds. It serves as a solvent, lubricant, and carrier in medicines, helping dissolve active ingredients and improve how the medication flows and absorbs in the body.
  • 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 415H64SACF
    A heat-loving bacterium used as a probiotic ingredient to support beneficial gut flora. It may help maintain digestive balance when included in supplements or certain foods.
  • UNII Q74T35078H
    Vanilla is a flavoring ingredient extracted from vanilla orchid beans. It's added to medicines to improve taste and make them more pleasant to take, especially for children or patients who need liquid formulations.
  • 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.

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

The official label also stateswater, caprylic/capric triglyceride, glycerin, cyclopentasiloxane, cetyl PEG/PPG-10/1 dimethicone, thermus thermophillus ferment, polyacrylate-13, cetearyl ethylhexanoate, phenoxyethanol, polyisobutene, polyglyceryl-6 polyricinoleate, lecithin, isostearic acid, polyglyceryl-3 polyricinoleate, polyhydroxystearic acid, soidum chloride, cetearyl dimethicone, marrubium vulgare extract, helianthus annus (sunflower) see oil, disteardimonium hectorite, polysorbate 20, citrus aurantum dulcis (orange) peel oil, limonene, sorbitan isostearate, ethylhexylglycerin, panthenol, citrus nobils (mandarin orange) peel oil, disodium EDTA, sodium hyaluronate, melanin, erythritol, citric acid, vanilla planifolia fruit extract, glycose, potassium sorbate, hydrolyzed pea protein, tocopherol, PEG-8/SMDI copolymer, tetrahexyldecyl ascoorbate, tocopheryl acetate, barosma betuuna (buchu) leaf oil, soidum benzoate, homarine HCL, pentaerythrityl tetra-di-t-butylhydroxyhydrocinnamate, sodium succinate, mallis domestica fruit cell culture extract, arabidopsis thaliana (thale cress) extract, micrococcus lysate, plankton extract, ergothioneine

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: 91 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
Image Skincare Prevention Plus Daily Ultimate Protection 100 g/1000g; 50 g/1000g; 60 g/1000g; 90 g/1000gthis 60232-1022-00 Swiss-American 7 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

🏛️
2020
On the market since
Jan 2020
📍
2026
Currently FDA-listed
6 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
60232-1022-00 You're viewing this 7 g in 1 TUBE (60232-1022-0) 2020-01-31 Active
60232-1022-03 91 g in 1 TUBE (60232-1022-3) 2020-01-31 Active

You're viewing the smallest of 2 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 60232-1022-00?
NDC 60232-1022-00 contains 7 g — 7 g in 1 tube.
What is the difference between NDC 60232-1022-00 and NDC 60232-1022-03?
Both are Image Skincare Prevention Plus Daily Ultimate Protection homosalate, octisalate, octocrylene, zinc oxide sunscreen 100 g/1000g; 50 g/1000g; 60 g/1000g; 90 g/1000g Cream — the drug itself is identical. NDC 60232-1022-00 is the 7 g package, while NDC 60232-1022-03 is the 91 g package.
What NDC number is used to bill for this package of Image Skincare Prevention Plus Daily Ultimate Protection homosalate, octisalate, octocrylene, zinc oxide sunscreen 100 g/1000g; 50 g/1000g; 60 g/1000g; 90 g/1000g Cream?
Bill NDC 60232-1022-00 — the 11-digit billing format is 60232102200. 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 — 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 60232-1022-0, 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: 60232-1022-00, written without dashes as 60232102200. 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 60232-1022-00, the first segment (60232) is the labeler code FDA assigned to Swiss-American CDMO, LLC; the middle segment (1022) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (00) 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 Swiss-American CDMO, 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 1 other package presentation of this same product, including 91 g (60232-1022-03). 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?
Swiss-American CDMO, 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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 29 words ▾

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

⏱️ Dosage and Administration 103 words ▾

Directions for Sunscreen Use Apply generously 15 minutes before sun exposure. Children under 6 months of age: ask a doctor. Reapply at least every 2 hours.

Use a water resistant sunscreen if swimming or sweating. Immediately after towel drying. At least every 2 hours.

Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: limit time in the sun, especially from 10am to 2pm, wear long-sleeved shirts, pants, hats and sunglasses.

⚠️ Warnings 48 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. If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 15 words ▾

Active Ingredients Homosalate 10.0% Sunscreen Octisalate 5.0% Sunscreen Octocrylene 6.0% Sunscreen Zinc Oxide 9.0% Sunscreen

🧪 Inactive Ingredients 114 words ▾

Inactive Ingredients water, caprylic/capric triglyceride, glycerin, cyclopentasiloxane, cetyl PEG/PPG-10/1 dimethicone, thermus thermophillus ferment, polyacrylate-13, cetearyl ethylhexanoate, phenoxyethanol, polyisobutene, polyglyceryl-6 polyricinoleate, lecithin, isostearic acid, polyglyceryl-3 polyricinoleate, polyhydroxystearic acid, soidum chloride, cetearyl dimethicone, marrubium vulgare extract, helianthus annus (sunflower) see oil, disteardimonium hectorite, polysorbate 20, citrus aurantum dulcis (orange) peel oil, limonene, sorbitan isostearate, ethylhexylglycerin, panthenol, citrus nobils (mandarin orange) peel oil, disodium EDTA, sodium hyaluronate, melanin, erythritol, citric acid, vanilla planifolia fruit extract, glycose, potassium sorbate, hydrolyzed pea protein, tocopherol, PEG-8/SMDI copolymer, tetrahexyldecyl ascoorbate, tocopheryl acetate, barosma betuuna (buchu) leaf oil, soidum benzoate, homarine HCL, pentaerythrityl tetra-di-t-butylhydroxyhydrocinnamate, sodium succinate, mallis domestica fruit cell culture extract, arabidopsis thaliana (thale cress) extract, micrococcus lysate, plankton extract, ergothioneine

🎯 Purpose 29 words ▾

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

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 60232-0046-01 · Swiss-American 60232-1026-06 · Swiss-American →
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.