Home › NDC Lookup › Ingredients › Octocrylene, Homosalate, Zinc Oxide, Oct... › 73071-0102-01
DEWYTREE URBAN SHADE INVISIBLE SMOOTHING PORE SUNSTIC SUNSTICK Octocrylene, Homosalate, Zinc Oxide, Octisalate 9.9 g/23.5g; 7.3 g/23.5g; 4.9 g/23.5g; 7.04 g/23.5g Stick, 23.5 g — NDC 73071-0102-01 package photo

DEWYTREE URBAN SHADE INVISIBLE SMOOTHING PORE SUNSTIC SUNSTICK Octocrylene, Homosalate, Zinc Oxide, Octisalate 9.9 g/23.5g; 7.3 g/23.5g; 4.9 g/23.5g; 7.04 g/23.5g Stick, 23.5 g

by DEWYTREE CO. ,LTD · 1 CONTAINER in 1 BOX (73071-102-01) / 23.5 g in 1 CONTAINER (73071-102-02)
NDC 73071-0102-01
🏷️ FDA NDC (as labeled) 73071-102-01 billing pads the product segment with a zero
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) 73071-102-01
Product NDC 73071-102
11-digit billing NDC 73071010201
UNII 5A68WGF6WM, V06SV4M95S, 4X49Y0596W, SOI2LOH54Z
Application # M020
SPL Set ID 48406e68-eefd-d2c2-e063-6394a90a4ad9
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-01-15
Route TOPICAL
Dosage form STICK
Substance OCTOCRYLENE; HOMOSALATE; OCTISALATE; ZINC OXIDE
Why two NDCs? The FDA registers this code as 73071-102-01 — 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 → 73071-0102-01. 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

LabelerDEWYTREE CO. ,LTD
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code73071
First marketedJan 2026
Product typeHuman Otc Drug
Portfolio2 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 sunscreen stick marketed as an over-the-counter monograph product. It contains four active ingredients that function as ultraviolet (UV) filters: homosalate, octisalate, and octocrylene are organic UV absorbers, while zinc oxide is a mineral UV reflectant. These ingredients are typically combined in sunscreen products to help block and scatter UV radiation from the sun. The stick form makes it convenient for targeted application to the face and other exposed areas.

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 purple
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 7QWA1RIO01
    A synthetic form of vitamin E used as an antioxidant in medicines. It prevents oils and fats in the formulation from breaking down, helping the drug remain stable and effective during storage.
  • 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 PQ6CK8PD0R
    Ascorbic acid, also known as vitamin C, is a white crystalline powder. It serves as an antioxidant to prevent degradation of other ingredients and may also function as a preservative in the formulation.
  • UNII 01YAE03M7J
    Beta carotene is a naturally occurring orange pigment found in plants. In medicines, it serves as a colorant to make tablets or capsules appear orange or yellow.
  • UNII 6SO6U10H04
    Biotin is a B-vitamin used as a nutritional supplement in some medications. It may also serve as a colorant or marker in formulations.
  • 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 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 60F80Z61A9
    A fragrant plant oil extracted from chamomile flowers. It's used as a flavoring agent and fragrance in medicines to improve taste and smell, making the product more pleasant to take.
  • UNII 8D9H4QU99H
    A synthetic fatty acid ester derived from coconut oil, used as an emulsifier and solubilizer to help mix oil and water-based ingredients and improve how the body absorbs certain drugs.
  • UNII Q9L0O73W7L
    Coconut oil is a natural fat extracted from coconut fruit. It's used in medicines as a lubricant, emollient, or carrier to help dissolve or deliver active ingredients smoothly through the formulation.
  • UNII 6BJQ43T1I9
    A synthetic peptide made from copper and amino acids. It's used in topical formulations as an active conditioning or skin-support ingredient, though classified as an excipient in some product listings.
  • UNII 0QW9S92J3K
    A plant-based oil extracted from Crambe abyssinica seeds. It acts as an emollient and skin-conditioning agent in topical formulations, helping to soften and smooth the product texture while improving how it spreads on skin.
  • UNII P6YC3EG204
    Cyanocobalamin is a synthetic form of vitamin B12. It's used in medicines as a nutritional ingredient and to help maintain the product's stability and potency over time.
  • UNII F4K100DXP3
    Dibutyl adipate is a synthetic oily liquid derived from adipic acid. It serves as a plasticizer and solvent in medicines, helping softens coatings and improves flexibility so tablets and capsules don't crack or break.
  • UNII 2865993309
    Ethylhexyl palmitate is an oily chemical made from palm oil and alcohol. It acts as an emollient and skin-conditioning agent in topical medicines, helping the product spread smoothly and keeping skin soft.
  • 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 935E97BOY8
    Folic acid is a synthetic form of a B vitamin. In medicines, it's added as a nutritional supplement or to help prevent vitamin deficiency, especially in prenatal formulas.
  • 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 IK8A76Q5G8
    A synthetic fatty acid derivative used as an emulsifier and preservative. It helps keep oil and water components mixed together in the formulation and protects the medicine from microbial growth.
  • UNII ZP9XFG71A7
    A plant extract from ivy leaves used as a natural ingredient. It may function as a preservative, emollient, or flavoring agent in medications and topical formulations.
  • 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 0K9R94573C
    A protein derived from pork collagen that has been broken down into smaller pieces using enzymes. It acts as a binder and thickener to help hold the medicine together and improve its texture and consistency.
  • UNII M30XO5X4XD
    A dried plant root extract from Florentine iris used as a natural fragrance, flavoring, and binding agent in medications. It helps hold tablet ingredients together and adds mild pleasant taste or aroma.
  • UNII 9I70D8O47I
    A plant-derived ingredient from the root of Lithospermum erythrorhizon. It may be used as a natural colorant or preservative in formulations.
  • UNII X72A60C9MT
    Lutein is a yellow-orange plant pigment from marigold flowers or synthesized chemically. It's used as a colorant to give medicines their yellow or orange appearance.
  • UNII EG97988M5Q
    A synthetic plastic polymer that forms a three-dimensional network. It's used as a coating on tablets and capsules to control how fast the medicine releases into the body, or as a binder to hold pill ingredients together.
  • UNII N8F53B3R4R
    A synthetic humectant and solvent derived from propane. It draws and holds moisture in the formulation, helping keep the medicine stable and improving texture or flow in liquid and semi-solid products.
  • UNII ZV095H5633
    A natural flavoring derived from muskmelon fruit. It is used in medicines to add pleasant taste and aroma, making the product more acceptable to take.
  • UNII 25X51I8RD4
    Niacinamide is a form of vitamin B3, a water-soluble nutrient. In medicines, it may be added as a nutritional supplement or to support skin health, though its primary role here is as an active ingredient rather than a traditional inactive filler.
  • UNII Q41S464P1R
    A synthetic peptide (short protein-like molecule) used in skincare and cosmetic formulations as an active conditioning ingredient to help improve skin texture and appearance. It may function as a humectant or skin-conditioning agent in topical products.
  • UNII RV743D216M
    A synthetic peptide derived from fatty acids and amino acids. It functions as a skin-conditioning agent and emollient in topical formulations, helping soften and smooth the product texture while supporting skin hydration.
  • UNII I9O0E3H2ZE
    Paraffin is a waxy, petroleum-derived substance used as a coating, lubricant, and hardening agent in tablets and capsules. It helps protect the medicine from moisture and gives pills a smooth finish.
  • UNII Y9WL8QN3ZB
    A plant-derived emulsifier made from glycerin and myristic acid. It helps mix oil and water-based ingredients together and keeps them blended throughout the product's shelf life.
  • UNII 15B05TY4GX
    A synthetic emulsifier derived from glycerin and oleic acid. It helps blend oil and water-based ingredients together in cosmetics and medicines, creating uniform, stable formulations.
  • UNII G4AYJ54K59
    A plant-derived emulsifier made from glycerin and oleic acid. It helps mix oil and water-based ingredients together and keeps them blended throughout the product's shelf life.
  • 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 03KCY6P7UT
    A waxy compound derived from cetyl alcohol and phosphoric acid. It acts as an emulsifier to help blend oil and water ingredients, and as a thickener to give the medicine its proper texture and consistency.
  • UNII KV2JZ1BI6Z
    Pyridoxine is a form of vitamin B6, a water-soluble vitamin. It's added to medicines as a nutritional supplement to help maintain adequate B6 levels in the body.
  • UNII 2ZN8DWC0YF
    A flavoring agent derived from pear fruit or created synthetically to mimic pear taste. It's added to medicines to improve flavor and make them more palatable, especially in liquid formulations for children.
  • UNII TLM2976OFR
    Riboflavin is a B vitamin used as a colorant and nutritional additive in medications. It gives products a yellow color and may provide supplemental vitamin B2 value.
  • UNII 18920M3T13
    Rosa damascena flower oil is a fragrant plant oil extracted from damask rose petals. It's used in medicines as a flavoring and aromatic agent to improve taste and scent.
  • UNII IJ67X351P9
    A natural plant extract from rosemary leaves used as a preservative to help prevent oils and fats in the medicine from spoiling or becoming rancid during storage.
  • UNII 836SJG51DR
    Sodium ascorbyl phosphate is a derivative of vitamin C that acts as an antioxidant and preservative in medications. It helps protect the drug's active ingredients from degradation caused by air and light exposure.
  • UNII M572600E5P
    Thiamine hydrochloride is a form of vitamin B1, a water-soluble nutrient. It's added to some medicines as a nutritional supplement or active ingredient component, though when listed as an excipient it typically serves as a stabilizer or minor additive in the formulation.
  • 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 9NH1UDD2RR
    A synthetic silicone polymer that forms a smooth, water-resistant film. Used in topical formulations as a skin protectant coating and to improve product texture and spreadability on the skin.
  • 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.

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

The official label also statesEthylhexyl Palmitate, Methyl Methacrylate Crosspolymer, Synthetic Wax, Vinyl Dimethi cone/Methicone Silsesquiox ane Crosspolymer, Caprylic/ Capric Triglyceride, Dibutyl Adipate, Butyloctyl Salicylat e, Crambe Abyssinica Seed Oil, 1,2-Hexanediol, Alpha-Bi sabolol, Polyhydroxystearic Acid, Polyglyceryl-4 Oleate, Pyrus Communis (Pear) Fruit Extract, Triethoxycaprylylsil ane, Tocopherol, Polyglycer yl-6 Oleate, Rosa Damascena Flower Water, Ethylhexylgly cerin, Iris Florentina Root Ex tract, Cucumis Melo (Melon) Fruit Extract, Hedera Helix (I vy) Leaf/Stem Extract, Beta -Carotene, Xanthophylls, Ro smarinus Officinalis (Rosema ry) Leaf Extract, Water, Glyc erin, Calamine, Butylene Gly col, Polyglyceryl-10 Myristat e, Hydrolyzed Extensin, Pot assium Cetyl Phosphate, Co cos Nucifera (Coconut) Oil, Methylpropanediol, Glycer yl Undecylenate, Coco-Cap rylate/Caprate, Copper T ripeptide-1, Palmitoyl Tetra peptide-7, Palmitoyl Tripep tide-1, Niacinamide, Sodium Ascorbyl Phosphate, Folic Acid, Thiamine HCl, Ribofla vin, Pyridoxine, Cyanocoba lamin, Biotin, Ascorbic Acid, Lactobacillus Ferment Ly sate, Lithospermum Erythro rhizon Root Extract, Chamo milla Recutita (Matricaria) Flower Oil, Helianthus Ann uus (Sunflower) Seed Oil

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 eachPer 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
Dewytree Urban Shade Invisible Smoothing Pore Sunstic Sunstick 9.9 g/23.5g; 7.3 g/23.5g; 4.9 g/23.5g; 7.04 g/23.5gthis 73071-0102-01 DEWYTREE 23.5 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

🏛️
2026
On the market since
Jan 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔒
·
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
73071-0102-01 You're viewing this 1 CONTAINER in 1 BOX (73071-102-01) / 23.5 g in 1 CONTAINER (73071-102-02) 2026-01-15 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 73071-102-01, 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: 73071-0102-01, written without dashes as 73071010201. 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 73071-0102-01, the first segment (73071) is the labeler code FDA assigned to DEWYTREE CO. ,LTD; the middle segment (0102) 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 DEWYTREE CO. ,LTD. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
DEWYTREE CO. ,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 32 words ▾

■ 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 87 words ▾

Directions ■ Apply liberally 15 minutes before sun exposure. ■ Reapply at least every 2 hours. ■ 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 10a.m.-2 p.m. wear long-sleeve shirts, pants, hats, and sunglasses.

⚠️ Warnings 5 words ▾

• For external use only.

🧪 Active Ingredient 9 words ▾

Homosalate 7.3% Octisalate 4.9% Octocrylene 9.9% Zinc Oxide 7.04%

🧪 Inactive Ingredients 148 words ▾

Ethylhexyl Palmitate, Methyl Methacrylate Crosspolymer, Synthetic Wax, Vinyl Dimethi cone/Methicone Silsesquiox ane Crosspolymer, Caprylic/ Capric Triglyceride, Dibutyl Adipate, Butyloctyl Salicylat e, Crambe Abyssinica Seed Oil, 1,2-Hexanediol, Alpha-Bi sabolol, Polyhydroxystearic Acid, Polyglyceryl-4 Oleate, Pyrus Communis (Pear) Fruit Extract, Triethoxycaprylylsil ane, Tocopherol, Polyglycer yl-6 Oleate, Rosa Damascena Flower Water, Ethylhexylgly cerin, Iris Florentina Root Ex tract, Cucumis Melo (Melon) Fruit Extract, Hedera Helix (I vy) Leaf/Stem Extract, Beta -Carotene, Xanthophylls, Ro smarinus Officinalis (Rosema ry) Leaf Extract, Water, Glyc erin, Calamine, Butylene Gly col, Polyglyceryl-10 Myristat e, Hydrolyzed Extensin, Pot assium Cetyl Phosphate, Co cos Nucifera (Coconut) Oil, Methylpropanediol, Glycer yl Undecylenate, Coco-Cap rylate/Caprate, Copper T ripeptide-1, Palmitoyl Tetra peptide-7, Palmitoyl Tripep tide-1, Niacinamide, Sodium Ascorbyl Phosphate, Folic Acid, Thiamine HCl, Ribofla vin, Pyridoxine, Cyanocoba lamin, Biotin, Ascorbic Acid, Lactobacillus Ferment Ly sate, Lithospermum Erythro rhizon Root Extract, Chamo milla Recutita (Matricaria) Flower Oil, Helianthus Ann uus (Sunflower) Seed Oil

🎯 Purpose 1 words ▾

Sunscreen

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 73071-0101-01 · DEWYTREE 73075-0001-01 · Isla →
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.