Skin On Skin BC Foundation SPF 40 - Fair Neutral octisalate, homosalate, zinc oxide 7 g/100mL; 3 g/100mL; 7 g/100mL Cream
by YENSA Beauty, LLC · 1 TUBE in 1 BOX (72782-104-30) / 30 mL in 1 TUBE
NDC 72782-0104-30
🏷️ FDA NDC (as labeled)
72782-104-30
billing pads the product segment with a zero
OTC
On market
Non-controlled
🗂️ Data synced Sep 17, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
🆔 Identity & classification
FDA NDC (as labeled)
72782-104-30
Product NDC
72782-104
11-digit billing NDC
72782010430
UNII
4X49Y0596W, SOI2LOH54Z, V06SV4M95S
Application #
M020
SPL Set ID
462e9a4a-ef28-0e0e-e063-6394a90ab4f8
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2025-07-01
Route
TOPICAL
Dosage form
CREAM
Substance
HOMOSALATE; OCTISALATE; ZINC OXIDE
Why two NDCs?
The FDA registers this code as 72782-104-30 — 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 → 72782-0104-30. 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
LabelerYENSA Beauty, LLC
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code72782
First marketedJul 2025
Product typeHuman Otc Drug
Portfolio16 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?
Skin On Skin BC Foundation SPF 40 is a topical cream foundation marketed as an over-the-counter drug under FDA's sunscreen monograph. It contains three active ingredients that function as ultraviolet (UV) filters: homosalate and octisalate are organic UV absorbers, while zinc oxide is an inorganic reflectant. These ingredients are typically used together in sunscreen products to help protect skin from both UVA and UVB radiation when applied to exposed skin.
Patient education
Supplement & herbal interactions
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.
💬 Questions about octisalate, homosalate, zinc oxide?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
🧪 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.
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UNII TR046Y3K1G
A liquid alcohol derived from petroleum or plant sources. It acts as a solvent and humectant in medicines, helping dissolve active ingredients and retain moisture in the formulation.
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UNII L4EL31FWIL
A synthetic peptide (short chain of amino acids) used as a conditioning or texture-enhancing agent in topical formulations. It helps improve product feel and skin compatibility in creams and lotions.
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UNII K72T3FS567
Adenosine is a naturally occurring nucleoside compound. In medicines, it functions as an active pharmaceutical ingredient in some formulations, though when listed as an excipient it may serve as a buffering or stabilizing agent to maintain product stability and pH.
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UNII C5INA23HXF
Arbutin is a natural compound found in plants that acts as a preservative in medicines. It helps prevent bacterial and fungal growth to keep the product stable and safe during storage.
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UNII D2EVP827PJ
A juice extract from aronia berries, a dark purple fruit. It's used as a natural colorant and flavoring agent to add color and taste to the medication.
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UNII 39W1PKE3JI
Bergamot oil is a citrus extract from bergamot orange peel. It's used as a flavoring and fragrance agent to improve taste and aroma in medicines.
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UNII BHW853AU9H
A natural compound found in plants like cloves and hops, beta-caryophyllene is used in medicines as a flavoring agent and to add aroma to the product.
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UNII 8A6OMU3I8L
A natural flavoring derived from blackberry fruit. It's added to medicines to improve taste and make them more pleasant to take.
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UNII F8XAG1755S
A plant-derived oil from borage seeds, rich in fatty acids. It's used in formulations as an emollient and skin-conditioning agent to help maintain moisture and improve texture.
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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.
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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.
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UNII 00YIU5438U
Caprylyl glycol is a clear liquid derived from coconut oil. In medicines, it acts as a humectant to retain moisture, a preservative booster to prevent microbial growth, and a solvent to help dissolve or mix other ingredients.
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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.
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UNII NU0OLX06F8
Chia seed is a plant-derived ingredient used as a binder and filler in medicines. It helps hold tablet or capsule ingredients together and adds bulk to the formulation.
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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.
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UNII H895X08VNQ
A silicone-based polymer that forms small, hard particles. It acts as a glidant and anti-caking agent to improve powder flow and prevent clumping in tablets and capsules.
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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.
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UNII VCA5491KVF
A fragrant oil extracted from clove leaves, used as a flavoring and aromatic agent to mask unpleasant tastes or add pleasant scent to medicines.
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UNII G7036X8B5H
A dark iron compound that gives medicine its color. Used as a colorant in tablets and capsules to help identify the medication and make it visually distinctive.
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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 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.
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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 7YR4ZFS62E
Hydrogenated polyisobutene is a synthetic, waxy polymer derived from petroleum. It acts as a lubricant and glidant in tablets and capsules, helping ingredients flow smoothly during manufacturing and preventing sticking.
-
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 WE98HW412B
A seaweed-derived ingredient from Japanese kelp. It acts as a thickener and binder in medications, helping create the proper texture and hold the formula together.
-
UNII ZBP1YXW0H8
A fragrant oil extracted from lavender plants, used as a flavoring and scent agent in medicines to improve taste and aroma.
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UNII CU2S39TB8O
A fungal material derived from shiitake mushroom growth. It may be used as a filler or binder to add bulk and help hold tablet or capsule ingredients together.
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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.
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UNII D81QY6I88E
Linalool is a natural fragrant oil found in plants like lavender and citrus. It's used in medicines as a flavoring agent and to mask unpleasant tastes or smells.
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UNII 5K47SSQ51G
A fragrant compound found in plants like lavender and bergamot. It's used as a flavoring and aroma agent to improve the taste and smell of medications.
-
UNII 6M3P64V0NC
A fine powder made from magnesium, aluminum, and silicon compounds. It absorbs moisture and helps keep medicine ingredients from clumping or separating, so the product stays stable and flows smoothly during manufacturing.
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UNII 4LVZ0Z0ITT
A plant seed ingredient used as a natural flavoring agent and filler. It adds taste and helps give the medicine its structure and volume.
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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.
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UNII 3K0J1S7QGC
A fragrant essential oil derived from geranium flowers, used as a flavoring and fragrance agent to improve the taste and aroma of medicines.
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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.
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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.
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UNII DR0K5NOJ4R
Phenyl trimethicone is a silicone-based lubricant and glidant. It helps powder particles flow smoothly and reduces friction during tablet or capsule manufacturing and filling.
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UNII 996299PUKB
Pinene is a natural oil compound found in pine trees and other plants. It's used in medicines as a flavoring agent and to help mask bitter or unpleasant tastes.
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UNII 687U3PEB2Y
A complex emulsifier made from glycerin and fatty acids. It helps blend oil and water-based ingredients together and improves the texture and stability of creams, lotions, and other formulated products.
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UNII 7N2B70SFEZ
Rice germ is the nutrient-rich inner layer of the rice grain. It's used in medicines as a filler and bulking agent to add volume and help bind ingredients together in tablets and capsules.
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UNII 7Y1255HVXR
A plant-derived oil from sesame seeds used as an emollient and solvent in topical formulations. It helps distribute active ingredients evenly and keeps products from drying out.
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UNII QX10HYY4QV
Sesame oil is a plant-derived oil from sesame seeds. It's used in medicines as a solvent or carrier to dissolve or suspend active ingredients, helping them mix evenly throughout the formulation.
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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.
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UNII 0W8RRI5W5A
A fatty acid derivative used as an emulsifier and surfactant in medications. It helps blend oily and water-based ingredients together to create a stable, uniform product.
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UNII OLX698AH5P
A clay mineral processed with a quaternary ammonium compound. It acts as a glidant and anti-caking agent to improve powder flow and prevent clumping in tablets and capsules.
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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.
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UNII Q3Z4BCH099
A manufactured wax made from refined petroleum or plant oils. It coats tablet surfaces to control how fast the medicine dissolves and releases, and improves how the tablet feels and looks.
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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.
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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.
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UNII LDC331P08E
A silicone-based compound that acts as a glidant and flow agent in solid medications. It reduces friction between powder particles, helping the medicine flow smoothly during manufacturing and tablet compression.
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UNII ICV1OK7M1S
A brown seaweed extract used as a thickener and stabilizer. It helps give medicines a smooth texture and keeps ingredients evenly mixed throughout the product.
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UNII X6M0DRN46Q
Urtica dioica leaf is a plant extract commonly used as a natural ingredient in dietary supplements and herbal formulations. It serves as an active botanical component intended to provide nutritional or herbal properties to the product.
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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.
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UNII 8YOY78GNNX
A fragrant essential oil derived from ylang-ylang tree flowers. It's used as a flavoring and fragrance agent to improve the taste or scent of medicines.
54 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statesWater, Isononyl Isononanoate, Hydrogenated Polyisobutene, Butylene Glycol, Cetyl PEG/PPG-10/1 Dimethicone, Caprylic/Capric Triglyceride, Arbutin, Phenyl Trimethicone, Synthetic Beeswax, Sorbitan Sesquioleate, Dimethicone, Sodium Chloride, Polyglyceryl-4 Diisostearate/Polyhydroxystearate/Sebacate, Stearalkonium Hectorite, Magnesium Aluminum Silicate, Caprylyl Glycol, Dimethicone/Vinyl Dimethicone Crosspolymer, Synthetic Wax, Triethoxycaprylylsilane, Pentylene Glycol, Borago Officinalis Seed Oil, Ethylhexylglycerin, Adenosine, Olea Europaea (Olive) Fruit Oil, Sesamum Indicum (Sesame) Seed Oil, Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Aronia Melanocarpa Fruit Extract, Camellia Sinensis Leaf Extract, Nigella Sativa Seed Extract, Laminaria Japonica Extract, Sesamum Indicum (Sesame) Seed Extract, Oryza Sativa (Rice) Extract, Rubus Fruticosus (Blackberry) Fruit Extract, Undaria Pinnatifida Extract, Lavandula Angustifolia (Lavender) Oil, Cananga Odorata Flower Oil, Citrus Aurantium Dulcis (Orange) Peel Oil, Cymbopogon Martini Oil, Pelargonium Graveolens Flower Oil, Salvia Hispanica Seed Extract, Lentinus Edodes Extract, Michelia Alba Leaf Oil, Eugenia Caryophyllus (Clove) Leaf Oil, Eucalyptus Globulus Leaf Oil, Urtica Dioica (Nettle) Extract, 1,2-Hexanediol, Michelia Alba Flower Oil, Tocopherol, Phenoxyethanol, Sodium Hyaluronate, Jasminum Grandiflorum (Jasmine) Flower Extract, Acetyl Hexapeptide-8, Titanium Dioxide, 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 system | Per g | Per 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
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
🏛️
2025
On the market since
Jul 2025
📍
2026
Currently FDA-listed
1 year 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 NDC | Description | Marketing start | Status |
|---|---|---|---|
| 72782-0104-30 You're viewing this | 1 TUBE in 1 BOX (72782-104-30) / 30 mL in 1 TUBE | 2025-07-01 | 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 | ✓ 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 72782-104-30, 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: 72782-0104-30, written without dashes as 72782010430. 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 72782-0104-30, the first segment (72782) is the labeler code FDA assigned to YENSA Beauty, LLC; the middle segment (0104) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (30) 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 YENSA Beauty, LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
YENSA Beauty, 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 ▾
Use helps prevent sunburn
⏱️ Dosage and Administration ▾
Directions For sunscreen use: apply liberally 15 minutes before sun exposure reapply at least every 2 hours use a water resistant sunscreen if swimming or sweating 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 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 10 a.m.-2 p.m. wear long-sleeved shirts, pants, hats, and sunglasses
⚠️ Warnings ▾
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.
🧪 Active Ingredient ▾
Active ingredients Octisalate 3% Homosalate 7% Zinc Oxide 7%
🧪 Inactive Ingredients ▾
Inactive ingredients Water, Isononyl Isononanoate, Hydrogenated Polyisobutene, Butylene Glycol, Cetyl PEG/PPG-10/1 Dimethicone, Caprylic/Capric Triglyceride, Arbutin, Phenyl Trimethicone, Synthetic Beeswax, Sorbitan Sesquioleate, Dimethicone, Sodium Chloride, Polyglyceryl-4 Diisostearate/Polyhydroxystearate/Sebacate, Stearalkonium Hectorite, Magnesium Aluminum Silicate, Caprylyl Glycol, Dimethicone/Vinyl Dimethicone Crosspolymer, Synthetic Wax, Triethoxycaprylylsilane, Pentylene Glycol, Borago Officinalis Seed Oil, Ethylhexylglycerin, Adenosine, Olea Europaea (Olive) Fruit Oil, Sesamum Indicum (Sesame) Seed Oil, Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Aronia Melanocarpa Fruit Extract, Camellia Sinensis Leaf Extract, Nigella Sativa Seed Extract, Laminaria Japonica Extract, Sesamum Indicum (Sesame) Seed Extract, Oryza Sativa (Rice) Extract, Rubus Fruticosus (Blackberry) Fruit Extract, Undaria Pinnatifida Extract, Lavandula Angustifolia (Lavender) Oil, Cananga Odorata Flower Oil, Citrus Aurantium Dulcis (Orange) Peel Oil, Cymbopogon Martini Oil, Pelargonium Graveolens Flower Oil, Salvia Hispanica Seed Extract, Lentinus Edodes Extract, Michelia Alba Leaf Oil, Eugenia Caryophyllus (Clove) Leaf Oil, Eucalyptus Globulus Leaf Oil, Urtica Dioica (Nettle) Extract, 1,2-Hexanediol, Michelia Alba Flower Oil, Tocopherol, Phenoxyethanol, Sodium Hyaluronate, Jasminum Grandiflorum (Jasmine) Flower Extract, Acetyl Hexapeptide-8, Titanium Dioxide, Iron Oxides
🎯 Purpose ▾
Purpose Sunscreen
No label section mentions that — try another word, or open the full label on DailyMed below.
Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA.
Prefer the government’s original formatting? View this label on DailyMed ↗
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.