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AVON ANEW SOLAIRE EVERYDAY FACE PROTECTION BROAD SPECTRUM SPF 50 SUNSCREEN Avobenzone, Homosalate, Octisalate, Octocrylene 4.5 g/50mL; 9 g/50mL; 2.7 g/50mL; 9 g/50mL Lotion — NDC 10096-2030-01 package photo

AVON ANEW SOLAIRE EVERYDAY FACE PROTECTION BROAD SPECTRUM SPF 50 SUNSCREEN Avobenzone, Homosalate, Octisalate, Octocrylene 4.5 g/50mL; 9 g/50mL; 2.7 g/50mL; 9 g/50mL Lotion

by THE AVON COMPANY · 1 TUBE in 1 BOX (10096-2030-1) / 50 mL in 1 TUBE
NDC 10096-2030-01
🏷️ FDA NDC (as labeled) 10096-2030-1 billing pads the package 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) 10096-2030-1
Product NDC 10096-2030
11-digit billing NDC 10096203001
UNII 4X49Y0596W, V06SV4M95S, G63QQF2NOX, 5A68WGF6WM
UPC 0888761749990
Application # M020
SPL Set ID 54f6d7c1-59d1-0b36-e063-6394a90a17a3
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-06-23
Route TOPICAL
Dosage form LOTION
Substance OCTISALATE; HOMOSALATE; AVOBENZONE; OCTOCRYLENE
Why two NDCs? The FDA registers this code as 10096-2030-1 — 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 → 10096-2030-01. 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

LabelerTHE AVON COMPANY
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code10096
First marketedJun 2026
Product typeHuman Otc Drug
Portfolio61 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 lotion sunscreen marketed as an over-the-counter monograph product. It contains four UV-filtering ingredients (avobenzone, homosalate, octisalate, and octocrylene) that are typically used together to absorb and scatter ultraviolet light across a broad spectrum. Products with this combination of filters are commonly applied to the face to help protect skin from sun exposure. The lotion formulation is designed for everyday topical use on skin.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

🧪 Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII 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 8Z5ZAL5H3V
    A synthetic polymer made from acrylate compounds. It acts as a thickener and stabilizer in topical formulations, helping create the right texture and prevent separation of ingredients.
  • UNII 298PX4M11X
    A synthetic chemical compound that acts as an antioxidant, helping protect the medicine's active ingredients from degradation caused by light, heat, and oxygen during storage and shelf life.
  • 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.
  • 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.
  • 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.
  • 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 2DMT128M1S
    A waxy solid derived from plant or animal sources. It acts as an emulsifier to blend oil and water components, and also thickens the medicine to give it the right texture and consistency.
  • UNII 58B69Q84JO
    A plant-derived emulsifier made from olive oil and fatty alcohols. It helps blend oil and water ingredients together and stabilizes the product's texture in creams, lotions, and similar formulations.
  • UNII T7EU0O9VPP
    Citral is a natural oil compound found in lemon and citrus plants. It's used in medicines as a flavoring agent and to add pleasant lemon or citrus scent to the product.
  • UNII P01OUT964K
    A fragrant plant-derived alcohol used as a flavoring agent and fragrance component in medicines. It provides taste and aroma to make the product more pleasant to use.
  • 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 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 L837108USY
    Geraniol is a natural fragrant compound found in plants like roses and lemons. It's used in medicines as a flavoring agent and to improve the taste or aroma of the product.
  • UNII 3W81YG7P9R
    Geranyl acetate is a fragrant compound derived from natural plant sources. It is used in medicines as a flavoring agent to improve taste or as a fragrance component.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII TM2TZD4G4A
    A plant-derived oily substance used as an emulsifier and solubilizer in medicines. It helps blend water and oil-based ingredients together and improves how the body absorbs certain active drugs.
  • UNII 230OU9XXE4
    A waxy substance made from glycerin and stearic acid that acts as an emulsifier to blend oily and watery ingredients together. It also helps thicken and stabilize the medicine's texture.
  • UNII 48RFF58ESG
    A plant-derived carbamate compound used as a binder and film-former in tablets and capsules. It helps hold ingredients together and may improve how the medicine breaks down in the digestive system.
  • UNII A8289P68Y2
    Isododecane is a lightweight liquid hydrocarbon used as a solvent and spreadability agent in topical formulations. It helps dissolve active ingredients and makes the product easier to apply and absorb into the skin.
  • UNII PAD4FN7P2G
    A fragrant essential oil from juniper wood, used primarily as a flavoring agent and fragrance component to mask tastes and add aroma to medicines.
  • UNII GFD7C86Q1W
    A natural oil extracted from citrus peels, (+)-limonene is used as a flavoring agent and solvent in medicines. It helps dissolve active ingredients and provides a lemon or orange taste.
  • UNII 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.
  • 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.
  • 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 AEE24M3MQ9
    Nutmeg is a natural spice derived from the seed of the nutmeg tree. It's used in medicines as a flavor ingredient to improve taste and mask unpleasant flavors in oral formulations.
  • UNII 3R834EPI82
    Paeonol is an organic compound derived from peony plant extract. It functions as an antioxidant and preservative in formulations, helping protect the medicine's stability and prevent degradation over time.
  • 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 3K0J1S7QGC
    A fragrant essential oil derived from geranium flowers, used as a flavoring and fragrance agent to improve the taste and aroma of medicines.
  • 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.
  • 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 1DGG9VW8SA
    Santalol is a natural alcohol extracted from sandalwood oil. It's used in medicines as a fragrance and flavoring agent to improve taste and smell.
  • UNII X7X01WMQ5F
    A fragrant oil derived from sandalwood trees, used primarily as a flavoring and scent agent in medicines to improve taste and aroma.
  • UNII MDL271E3GR
    Sorbitan olivate is an emulsifier derived from sorbitol and olive oil. It helps blend water and oil ingredients together to maintain consistent texture and appearance throughout the medicine.
  • UNII R53Q4ZWC99
    Terpineol is a fragrant alcohol derived from pine oil or other plant sources. It's used in medicines as a flavoring agent and to improve the taste or aroma of the product.
  • UNII N9830X5KSL
    Terpinolene is a natural aromatic compound found in plants. It's used in medicines as a flavoring agent to improve taste and scent.
  • UNII 420IP921MB
    A chelating agent derived from edetic acid that binds to metals in the formulation. It helps stabilize the medicine by preventing metal ions from causing breakdown or discoloration.
  • UNII 023C2WHX2V
    Tromethamine is a chemical buffer that helps maintain the proper acidity level in liquid medicines. It neutralizes acids and stabilizes the solution so the medication remains effective and safe throughout its shelf life.
  • 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.

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

The official label also statesWATER, GLYCERIN, DIMETHICONE, CETEARYL ALCOHOL, ISODODECANE, POTASSIUM CETYL PHOSPHATE, ACRYLATES/ POLYTRIMETHYLSILOXYMETHACRYLATE COPOLYMER, 1,2-HEXANEDIOL, BENZOTRIAZOLYL DODECYL P-CRESOL, PANTHENOL, GLYCERYL CAPRYLATE, GLYCERYL STEARATE, NIACINAMIDE, CAPRYLIC/CAPRIC TRIGLYCERIDE, MAGNESIUM ALUMINUM SILICATE, CETEARYL OLIVATE, INULIN LAURYL CARBAMATE, FRAGRANCE, SORBITAN OLIVATE, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, XANTHAN GUM, DIPROPYLENE GLYCOL, TROMETHAMINE, TRISODIUM EDTA, MYRISTICA FRAGRANS (NUTMEG) EXTRACT, PAEONOL, PAEONIA SUFFRUTICOSA BRANCH/FLOWER/LEAF EXTRACT, CITRUS AURANTIUM BERGAMIA PEEL OIL, LIMONENE, LINALYL ACETATE, PINENE, LINALOOL, CITRAL, TERPINOLENE, GERANIOL, GERANYL ACETATE, BETA-CARYOPHYLLENE, TERPINEOL, CITRONELLOL, CANANGA ODORATA OIL/EXTRACT, JUNIPERUS VIRGINIANA OIL, PELARGONIUM GRAVEOLENS FLOWER OIL, SANTALOL, SANTALUM ALBUM 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 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
belif The true cream aqua bomb sunscreen Broad Spectrum SPF 45 4.5 g/50mL; 9 g/50mL; 2.7 g/50mL; 9 g/50mL 72330-0722-10 fmg 1 tube — — FDA listed —
Isa Knox Anew Solaire Everyday Face Protection Broad Spectrum Spf 50 Sunscreen 4.5 g/50mL; 9 g/50mL; 2.7 g/50mL; 9 g/50mL 53208-0203-01 LG 2 tubes — — FDA listed —
Isa Knox Anew Solaire Everyday Face Protection Broad Spectrum Spf 50 Sunscreen 4.5 g/50mL; 9 g/50mL; 2.7 g/50mL; 9 g/50mL 53208-0201-01 LG 2 tubes — — FDA listed —
CNP Laboratory Sun Care Milky Light Sunscreen Broad Spectrum SPF 50 4.5 g/50mL; 9 g/50mL; 2.7 g/50mL; 9 g/50mL 72330-0101-50 fmg 1 tube — — FDA listed —
Isa Knox Anew Solaire Active Face And Body Protection Broad Spectrum Spf 50 Sunscreen 4.5 g/50mL; 9 g/50mL; 2.7 g/50mL; 9 g/50mL 72330-0502-01 fmg 2 tubes — — FDA listed —
Isa Knox Anew Solaire Everyday Face Protection Broad Spectrum Spf 50 Sunscreen 4.5 g/50mL; 9 g/50mL; 2.7 g/50mL; 9 g/50mL 72330-0503-01 fmg 2 tubes — — FDA listed —
Isa Knox Anew Solaire Active Face And Body Protection Broad Spectrum Spf 50 Sunscreen 4.5 g/50mL; 9 g/50mL; 2.7 g/50mL; 9 g/50mL 53208-0202-01 LG 2 tubes — — FDA listed —
belif The true cream aqua bomb sunscreen Broad Spectrum SPF 50 4.5 g/50mL; 9 g/50mL; 2.7 g/50mL; 9 g/50mL 53208-0710-01 LG 2 tubes — — FDA listed —
belif The true cream aqua bomb sunscreen Broad Spectrum SPF 45 4.5 g/50mL; 9 g/50mL; 2.7 g/50mL; 9 g/50mL 53208-0721-50 LG 1 tube — — FDA listed —
Isa Knox Anew Solaire Everyday Face Protection Broad Spectrum Spf 50 Sunscreen 4.5 g/50mL; 9 g/50mL; 2.7 g/50mL; 9 g/50mL 72330-0501-01 fmg 2 tubes — — FDA listed —
belif The true cream aqua bomb sunscreen Broad Spectrum SPF 45 4.5 g/50mL; 9 g/50mL; 2.7 g/50mL; 9 g/50mL 72330-0721-50 fmg 1 tube — — FDA listed —
Dominas Dark Spot UV Defense Sunscreen Broad Spectrum SPF 50 4.5 g/50mL; 9 g/50mL; 2.7 g/50mL; 9 g/50mL 53208-0301-50 LG 1 tube — — FDA listed —
CNP Laboratory Sun Care Milky Light Sunscreen Broad Spectrum SPF 50 4.5 g/50mL; 9 g/50mL; 2.7 g/50mL; 9 g/50mL 53208-0101-50 LG 1 tube — — FDA listed —
belif The true cream aqua bomb sunscreen Broad Spectrum SPF 45 4.5 g/50mL; 9 g/50mL; 2.7 g/50mL; 9 g/50mL 53208-0722-10 LG 1 tube — — FDA listed —
belif The true cream aqua bomb sunscreen Broad Spectrum SPF 50 4.5 g/50mL; 9 g/50mL; 2.7 g/50mL; 9 g/50mL 72330-0710-01 fmg 2 tubes — — FDA listed —
Avon Anew Solaire Everyday Face Protection Broad Spectrum Spf 50 Sunscreen 4.5 g/50mL; 9 g/50mL; 2.7 g/50mL; 9 g/50mLthis 10096-2030-01 THE 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

🏛️
2026
On the market since
Jun 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.

🔬 Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for AVON ANEW SOLAIRE EVERYDAY FACE PROTECTION BROAD SPECTRUM SPF 50 SUNSCREEN (this brand).

Top reported reactions

Acute Myeloid Leukaemia2
Exposure To Toxic Agent2
Product Contamination Chemical2
Rash2
Anaphylactic Reaction1
Application Site Erythema1
Application Site Exfoliation1

Age at onset

Adolescent2
Adult1

Reporter sex

6 reports
Male · 20%
Female · 80%

Serious outcomes

Hospitalization2
Life-threatening1
Death1
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
10096-2030-01 You're viewing this 1 TUBE in 1 BOX (10096-2030-1) / 50 mL in 1 TUBE 2026-06-23 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 10096-2030-1, 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: 10096-2030-01, written without dashes as 10096203001. 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 10096-2030-01, the first segment (10096) is the labeler code FDA assigned to THE AVON COMPANY; the middle segment (2030) 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 THE AVON COMPANY. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
THE AVON COMPANY is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.

📄 FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 30 words ▾

USES helps prevent sunburn if used as directed with other sun protection measures (see Directions ), decreases the risk of skin cancer and early skin aging caused by the sun

⏱️ Dosage and Administration 94 words ▾

DIRECTIONS For sunscreen use: apply liberally 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 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 5 words ▾

WARNINGS For external use only

📦 Storage and Handling 22 words ▾

OTHER INFORMATION protect the product in this container from excessive heat and direct sun the product may stain certain types of fabrics

🧪 Active Ingredient 10 words ▾

ACTIVE INGREDIENTS Avobenzone 2.7% Homosalate 9.0% Octisalate 4.5% Octocrylene 9.0%

🧪 Inactive Ingredients 89 words ▾

INACTIVE INGREDIENTS WATER, GLYCERIN, DIMETHICONE, CETEARYL ALCOHOL, ISODODECANE, POTASSIUM CETYL PHOSPHATE, ACRYLATES/ POLYTRIMETHYLSILOXYMETHACRYLATE COPOLYMER, 1,2-HEXANEDIOL, BENZOTRIAZOLYL DODECYL P-CRESOL, PANTHENOL, GLYCERYL CAPRYLATE, GLYCERYL STEARATE, NIACINAMIDE, CAPRYLIC/CAPRIC TRIGLYCERIDE, MAGNESIUM ALUMINUM SILICATE, CETEARYL OLIVATE, INULIN LAURYL CARBAMATE, FRAGRANCE, SORBITAN OLIVATE, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, XANTHAN GUM, DIPROPYLENE GLYCOL, TROMETHAMINE, TRISODIUM EDTA, MYRISTICA FRAGRANS (NUTMEG) EXTRACT, PAEONOL, PAEONIA SUFFRUTICOSA BRANCH/FLOWER/LEAF EXTRACT, CITRUS AURANTIUM BERGAMIA PEEL OIL, LIMONENE, LINALYL ACETATE, PINENE, LINALOOL, CITRAL, TERPINOLENE, GERANIOL, GERANYL ACETATE, BETA-CARYOPHYLLENE, TERPINEOL, CITRONELLOL, CANANGA ODORATA OIL/EXTRACT, JUNIPERUS VIRGINIANA OIL, PELARGONIUM GRAVEOLENS FLOWER OIL, SANTALOL, SANTALUM ALBUM OIL.

🎯 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 ↗
← 10096-2020-01 · THE 10096-2120-01 · THE →
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.