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Sheglam Dew and Done Skin Tint with SPF 20 Wheat ZINC OXIDE 146.25 mg/mL Cream — NDC 85068-0035-01 package photo

Sheglam Dew and Done Skin Tint with SPF 20 Wheat ZINC OXIDE 146.25 mg/mL Cream

by EVER FAME PTE. LTD. · 1 TUBE in 1 CARTON (85068-035-01) / 30 mL in 1 TUBE
NDC 85068-0035-01
🏷️ FDA NDC (as labeled) 85068-035-01 billing pads the product segment with a zero
OTC On market Non-controlled
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

⚠️
Other active recalls for Zinc Oxide (different manufacturers) — 6 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0212-2026
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0206-2026
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0202-2026
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0207-2026
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0209-2026
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0208-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

🆔 Identity & classification

FDA NDC (as labeled) 85068-035-01
Product NDC 85068-035
11-digit billing NDC 85068003501
UNII SOI2LOH54Z
Application # M020
SPL Set ID 2acf92a1-6d2a-5517-e063-6294a90a7488
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 2025-05-30
Route TOPICAL
Dosage form CREAM
Substance ZINC OXIDE
Why two NDCs? The FDA registers this code as 85068-035-01 — 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 → 85068-0035-01. 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

LabelerEVER FAME PTE. LTD.
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code85068
First marketedMay 2025
Product typeHuman Otc Drug
Portfolio35 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 skin tint cream that contains zinc oxide, a mineral ingredient typically used in sunscreen products to help protect skin from ultraviolet (UV) rays. Zinc oxide functions as a physical UV filter that sits on the skin surface to reflect and scatter UV light. The product is marketed as an over-the-counter monograph drug, meaning it is formulated under FDA's established rules for sunscreen products rather than as an individually approved application.

Supplement & herbal interactions

Some supplements/herbs that may interact with Zinc oxide (OTC drug) — tap one for details:

Dimethylsulfoxide (dmso)Moderate Turpentine OilModerate AlchemillaMinor
🌿 Every supplement checked against Zinc oxide (OTC drug) (3 interactions) — ranked by severity →
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 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.
  • UNII 8XWR7NN42F
    A sugar alcohol derived from natural sources, used as a sweetener and filler in medicines. It helps improve taste and provides bulk to tablets and powders without adding significant calories.
  • UNII 24WE03BX2T
    Levomenol is a naturally derived alcohol compound used as a skin-conditioning and anti-inflammatory agent in topical formulations. It helps soothe and protect the skin while improving product texture and absorption.
  • 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 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 7J5R5W72QM
    C9-12 alkane is a clear, colorless liquid hydrocarbon mixture derived from petroleum. In medicines, it serves as a solvent, lubricant, or component in liquid formulations to help dissolve or suspend active ingredients.
  • UNII Q95M2P1KJL
    A silicone-based ingredient that acts as a lubricant and glidant. It helps the tablet or capsule move smoothly through manufacturing equipment and improves powder flow during production.
  • 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 21AS8B1BSS
    A silicone-based ingredient that combines dimethicone (silicone oil) with polyethylene glycol. It works as a skin-conditioning agent and texture enhancer, helping smooth the product's feel and improve how it spreads on skin.
  • UNII E107L85C40
    Dipropylene glycol is a clear liquid made from propylene glycol. It acts as a solvent and humectant in medicines, helping dissolve active ingredients and retain moisture in the formulation.
  • 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 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 C5529G5JPQ
    Ginger is a plant-derived ingredient used as a flavoring agent to add taste and aroma to medicines. It may also provide mild soothing properties to support product palatability.
  • 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 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 724GKU717M
    Jojoba oil is a natural liquid wax extracted from jojoba plant seeds. It's used in medicines as an emollient and lubricant to soften and smooth the product, and sometimes as a carrier or penetration enhancer.
  • UNII DE08037SAB
    Magnesium sulfate is a mineral salt that acts as an osmotic agent in medications. It draws water into the intestines to soften stool or is used as a filler and processing aid in some solid dosage forms.
  • UNII SST9XCL51M
    Oryzanol is a plant compound extracted from rice bran oil. It's used in medicines as an antioxidant and emollient to help stabilize the formula and improve texture.
  • UNII 1Q73Q2JULR
    Sodium citrate is a salt derived from citric acid. It works as a buffer to maintain the medicine's pH level and may also help improve taste or act as a preservative in 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 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 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.
  • 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 VCQ006KQ1E
    Xylitol is a naturally occurring sugar alcohol derived from plants. It's used in medicines as a sweetener, bulking agent, and to improve taste, especially in liquid formulations and chewable tablets.
  • UNII O0IEZ166FB
    A natural sugar substitute derived from plant sources, used as a sweetener and humectant to improve taste and help retain moisture in the medication.

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

The official label also statesWater, Glycerin, Dimethicone, Caprylyl Methicone, C9-12 Alkane, Butylene Glycol, Butyloctyl Salicylate, Dimethicone/PEG-10/15 Crosspolymer, Trimethylsiloxysilicate, Jojoba Seed Oil, Oryzanol, Isononyl Isononanoate, Magnesium Sulfate, 1,2-Hexanediol, PEG-10 Dimethicone, Hydroxyacetophenone, Triethoxycaprylylsilane, Sodium Hyaluronate, Dipropylene Glycol, Sodium Citrate, Gotu Kola Leaf Extract, Bisabolol, Tocopherol, Snow Lotus Extract, Xylitylglucoside, Anhydroxylitol, Xylitol, Ethylhexylglycerin, Ginger Root Extract, Titanium Dioxide Color, Iron Oxides Color.

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.
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
Sheglam Dew and Done Skin Tint with SPF 20 Cocoa 146.25 mg/mL 85068-0011-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Dark Clove 146.25 mg/mL 85068-0012-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Sepia 146.25 mg/mL 85068-0030-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Almond 146.25 mg/mL 85068-0001-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Butter 146.25 mg/mL 85068-0003-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Camel 146.25 mg/mL 85068-0005-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Saddle 146.25 mg/mL 85068-0027-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Chesnut 146.25 mg/mL 85068-0010-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Hazelnut 146.25 mg/mL 85068-0017-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Mocha 146.25 mg/mL 85068-0021-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Sand 146.25 mg/mL 85068-0028-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Mahogany 146.25 mg/mL 85068-0020-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Sandalwood 146.25 mg/mL 85068-0029-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Wheat 146.25 mg/mLthis 85068-0035-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Bamboo 146.25 mg/mL 85068-0002-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Linen 146.25 mg/mL 85068-0019-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Nude 146.25 mg/mL 85068-0022-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Walnut 146.25 mg/mL 85068-0033-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Cashew 146.25 mg/mL 85068-0008-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Deep Coffee 146.25 mg/mL 85068-0013-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Earth 146.25 mg/mL 85068-0014-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Fair 146.25 mg/mL 85068-0015-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Golden 146.25 mg/mL 85068-0016-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Truffle 146.25 mg/mL 85068-0032-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Caramel 146.25 mg/mL 85068-0007-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Shell 146.25 mg/mL 85068-0031-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Warm Vanilla 146.25 mg/mL 85068-0034-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Cappuchino 146.25 mg/mL 85068-0006-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Butterscotch 146.25 mg/mL 85068-0004-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Chantilly 146.25 mg/mL 85068-0009-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Honey 146.25 mg/mL 85068-0018-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Nutmeg 146.25 mg/mL 85068-0023-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Peach 146.25 mg/mL 85068-0024-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Porcelain 146.25 mg/mL 85068-0025-01 EVER 1 tube — — FDA listed —
Sheglam Dew and Done Skin Tint with SPF 20 Russet 146.25 mg/mL 85068-0026-01 EVER 1 tube — — 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

🏛️
2025
On the market since
May 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 NDCDescription Marketing startStatus
85068-0035-01 You're viewing this 1 TUBE in 1 CARTON (85068-035-01) / 30 mL in 1 TUBE 2025-05-30 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 85068-035-01, 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: 85068-0035-01, written without dashes as 85068003501. 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 85068-0035-01, the first segment (85068) is the labeler code FDA assigned to EVER FAME PTE. LTD.; the middle segment (0035) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) 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 EVER FAME PTE. LTD.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
EVER FAME PTE. LTD. 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 4 words ▾

Use helps prevent sunburn

⏱️ Dosage and Administration 32 words ▾

Directions 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

⚠️ Warnings 90 words ▾

Warnings Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn, not skin cancer or early skin aging. For external use only.

Do not use on damaged or broken skin. When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if rash occurs. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 7 words ▾

Active ingredient Zinc Oxide 14.625% Purpose Sunscreen

🧪 Inactive Ingredients 57 words ▾

Inactive ingredients Water, Glycerin, Dimethicone, Caprylyl Methicone, C9-12 Alkane, Butylene Glycol, Butyloctyl Salicylate, Dimethicone/PEG-10/15 Crosspolymer, Trimethylsiloxysilicate, Jojoba Seed Oil, Oryzanol, Isononyl Isononanoate, Magnesium Sulfate, 1,2-Hexanediol, PEG-10 Dimethicone, Hydroxyacetophenone, Triethoxycaprylylsilane, Sodium Hyaluronate, Dipropylene Glycol, Sodium Citrate, Gotu Kola Leaf Extract, Bisabolol, Tocopherol, Snow Lotus Extract, Xylitylglucoside, Anhydroxylitol, Xylitol, Ethylhexylglycerin, Ginger Root Extract, Titanium Dioxide Color, Iron Oxides Color.

🎯 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 ↗
← 85068-0034-01 · EVER 85090-0001-01 · Good →
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.