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ARTISTRY YOUTH XTEND Lifting Smoothing Foundation Broad Spectrum SPF 20 Sunscreen OCTINOXATE, OXYBENZONE 75 mg/mL; 5 mg/mL Cream, 30 mL

by Amway Corp · 30 mL in 1 BOTTLE (50390-111-00)
NDC 50390-0111-00
🏷️ FDA NDC (as labeled) 50390-111-00 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

🆔 Identity & classification

FDA NDC (as labeled) 50390-111-00
Product NDC 50390-111
11-digit billing NDC 50390011100
UNII 4Y5P7MUD51, 95OOS7VE0Y
Application # M020
SPL Set ID 8cde14ae-b886-4bd2-b2bd-db604373984a
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2013-05-06
Route TOPICAL
Dosage form CREAM
Substance OCTINOXATE; OXYBENZONE
Why two NDCs? The FDA registers this code as 50390-111-00 — 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 → 50390-0111-00. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

🏭 Manufacturer & labeler

LabelerAmway Corp
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code50390
First marketedMay 2013
Product typeHuman Otc Drug
Portfolio40 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

🩺 Clinical

🧪 What is this product?

This is an over-the-counter monograph sunscreen product formulated as a cream applied to the skin. It contains two active ingredients, octinoxate and oxybenzone, which are ultraviolet (UV) filters commonly used in sunscreen products to help protect skin from sun exposure. The product is labeled with a Broad Spectrum SPF 20 rating and is marketed as a foundation with lifting and smoothing cosmetic properties.

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 S347WMO6M4
    Beta-sitosterol is a plant-derived sterol (waxy substance from vegetable oils and seeds). In medicines, it acts as an emulsifier or thickening agent to help blend oil and water-based ingredients and improve texture.
  • UNII 3M7W78X5IR
    A synthetic compound made by combining a short protein fragment (dipeptide) with fatty acid chains. It acts as an emulsifier and texture enhancer, helping oil and water blend smoothly in creams and lotions.
  • UNII 5QB0T2IUN0
    Aluminum hydroxide is a white powder mineral compound used as an antacid ingredient in some formulations. It works as a buffer and pH regulator to help neutralize stomach acid in the medicine.
  • UNII 4ZR792I587
    Bismuth oxychloride is a white powder derived from bismuth metal. In medicines, it's used mainly as a colorant and opacifying agent to give tablets or capsules their appearance and to make liquid formulations less transparent.
  • UNII 4370DF050B
    Ceramide NP is a waxy, lipid-based substance that mimics natural skin oils. It's used in topical formulations as an emollient and skin-conditioning agent to help soften, smooth, and protect the skin barrier.
  • UNII MC2LH51BO7
    A plant-derived oil extracted from chia seeds, used as an emollient and vehicle in topical or oral formulations. It helps deliver active ingredients and may improve product texture or absorption.
  • UNII RYQ4R60M02
    A green algae ingredient used as a natural colorant and nutritional filler in supplements and medications. It adds color and bulk to tablets and capsules.
  • UNII 0THT5PCI0R
    A silicone-based liquid that helps distribute active ingredients evenly throughout topical products. It acts as a solvent and emollient, allowing medicines to spread smoothly on skin while improving texture and absorption.
  • UNII 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 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 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 25G622K2RA
    A silicone-based surfactant that helps blend oil and water in cosmetic or topical formulations. It reduces surface tension to improve product spreadability and texture.
  • UNII 412ZHA4T4Y
    A plant-derived oil extracted from meadowfoam seeds. It acts as an emollient and skin-conditioning agent, helping soften and smooth the product texture while improving how it spreads on skin.
  • UNII S73ZQI0GXM
    Methyl trimethicone is a silicone-based lubricant and glidant used in tablets and capsules. It reduces friction between particles and equipment during manufacturing, helping the medicine flow smoothly and compress evenly.
  • UNII A2I8C7HI9T
    Methylparaben is a preservative derived from benzoic acid that prevents growth of bacteria, fungi, and mold in medicines. It extends the product's shelf life and maintains safety during storage.
  • UNII 322MS57V7Z
    A plant-derived oil from perilla seeds. It's used as an emollient and skin-conditioning agent to help soften and smooth the product's texture.
  • UNII Z8IX2SC1OH
    Propylparaben is a chemical preservative used to prevent bacterial and fungal growth in medicines and personal care products. It helps extend shelf life and maintain product safety during storage.
  • UNII 241ATL177A
    Soybean oil is a natural plant oil derived from soybean seeds. It's used in medicines as a solvent and carrier to help dissolve or suspend active ingredients and improve how the body absorbs them.
  • UNII 4ELV7Z65AP
    Stearic acid is a fatty acid derived from plant or animal sources. It acts as a binder and lubricant in tablets and capsules, helping them hold together and flow smoothly during manufacturing.
  • UNII 7SEV7J4R1U
    A powder made from a naturally occurring mineral. In medicines, talc works as a glidant and anti-caking agent, helping tablets and capsules flow smoothly during manufacturing and preventing clumping.
  • UNII 9LBV3F07AZ
    A synthetic, oil-soluble form of vitamin C used as an antioxidant to prevent degradation of the medicine and maintain its stability during storage.
  • UNII 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 N1TRQ06KVJ
    A synthetic oily compound used as a solvent and penetration enhancer in medicines. It helps dissolve active ingredients and improves absorption through the skin or mucous membranes in topical and transdermal formulations.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.

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

The official label also statesWATER/AQUA/EAU, CYCLOPENTASILOXANE, METHYL TRIMETHICONE, BUTYLENE GLYCOL, GLYCERIN, LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE, TALC, DIMETHICONE, TRIMETHYLOLPROPANE TRICAPRYLATE/TRICAPRATE, POLYGLYCERYL-6 POLYRICINOLEATE, HDI/ TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER, DIMETHICONE/PEG-10/15 CROSSPOLYMER, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, PHENOXYETHANOL, SODIUM CHLORIDE, SODIUM CITRATE, POLYGLYCERYL- 3 POLYDIMETHYLSILOXYETHYL DIMETHICONE, TRIETHOXYCAPRYLYLSILANE, ALUMINA, SORBITAN LAURATE, ALUMINUM HYDROXIDE, STEARIC ACID, METHYLPARABEN, SODIUM HYALURONATE, PROPYLPARABEN, FRAGRANCE/ PARFUM, HYDROXYETHYLCELLULOSE, ACETYL DIPEPTIDE-1 CETYL ESTER, ETHYLPARABEN, SILICA, IODOPROPYNYL BUTYLCARBAMATE, LECITHIN, CHLORELLA VULGARIS EXTRACT, GLYCINE SOJA (SOYBEAN) OIL, CERAMIDE-3, LIMNANTHES ALBA (MEADOWFOAM) SEED OIL, BETA-SITOSTEROL, PERILLA OCYMOIDES SEED OIL, SALVIA HISPANICA SEED OIL, OENOTHERA BIENNIS (EVENING PRIMROSE) OIL, TETRAHEXYLDECYL ASCORBATE. MAY CONTAIN/PEUT CONTEINIR:TITANIUM DIOXIDE, IRON OXIDES, BISMUTH OXYCHLORIDE

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
ARTISTRY YOUTH XTEND Lifting Smoothing Foundation Broad Spectrum SPF 20 Sunscreen 75 mg/mL; 5 mg/mLthis 50390-0111-00 Amway 30 ml — — FDA listed —
Artistry Youth Xtend Lifting Smoothing Foundation Shade Buff L1W1 75 mg/mL; 5 mg/mL 50390-0227-00 Amway 1 bottle — — FDA listed —
Artistry Youth Xtend Lifting Smoothing Foundation Shade Chablis L1C1 75 mg/mL; 5 mg/mL 50390-0228-00 Amway 1 bottle — — FDA listed —
Artistry Youth Xtend Lifting Smoothing Foundation Shade Cream L1W2 75 mg/mL; 5 mg/mL 50390-0229-00 Amway 1 bottle — — FDA listed —
Artistry Youth Xtend Lifting Smoothing Foundation Shade Mink L6W1 75 mg/mL; 5 mg/mL 50390-0230-00 Amway 1 bottle — — FDA listed —
Artistry Youth Xtend Lifting Smoothing Foundation Shade Ochre L2N1 75 mg/mL; 5 mg/mL 50390-0231-00 Amway 1 bottle — — FDA listed —
Artistry Youth Xtend Lifting Smoothing Foundation Shade Sand L2W1 75 mg/mL; 5 mg/mL 50390-0232-00 Amway 1 bottle — — FDA listed —
Artistry Youth Xtend Lifting Smoothing Foundation Shade Soleil L3W1 75 mg/mL; 5 mg/mL 50390-0233-00 Amway 1 bottle — — FDA listed —
Artistry Youth Xtend Lifting Smoothing Foundation Shade Tawny L3N1 75 mg/mL; 5 mg/mL 50390-0234-00 Amway 1 bottle — — FDA listed —
Artistry Youth Xtend Lifting Smoothing Foundation Shade Walnut L6N1 75 mg/mL; 5 mg/mL 50390-0235-00 Amway 1 bottle — — FDA listed —
Artistry Youth Xtend Lifting Smoothing Foundation Shade Brule L4W1 75 mg/mL; 5 mg/mL 50390-0236-00 Amway 1 bottle — — FDA listed —
Artistry Youth Xtend Lifting Smoothing Foundation Shade Cappuccino L5W1 75 mg/mL; 5 mg/mL 50390-0237-00 Amway 1 bottle — — FDA listed —
Artistry Youth Xtend Lifting Smoothing Foundation Shade Caramel L5N1 75 mg/mL; 5 mg/mL 50390-0238-00 Amway 1 bottle — — FDA listed —
Artistry Youth Xtend Lifting Smoothing Foundation Shade Chiffon L2C1 75 mg/mL; 5 mg/mL 50390-0239-00 Amway 1 bottle — — FDA listed —
Artistry Youth Xtend Lifting Smoothing Foundation Shade Golden L4N1 75 mg/mL; 5 mg/mL 50390-0240-00 Amway 1 bottle — — FDA listed —
Artistry Youth Xtend Lifting Smoothing Foundation Shade Natural L2N2 75 mg/mL; 5 mg/mL 50390-0241-00 Amway 1 bottle — — FDA listed —
Artistry Youth Xtend Lifting Smoothing Foundation Shade Plush L3C1 75 mg/mL; 5 mg/mL 50390-0242-00 Amway 1 bottle — — 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

🏛️
2013
On the market since
May 2013
📍
2026
Currently FDA-listed
13 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

🔬 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 OCTINOXATE, OXYBENZONE — the ingredient across all brands.

Top reported reactions

Dyspnoea2
Swelling Face2
Application Site Exfoliation1
Application Site Pain1
Application Site Swelling1
Burning Sensation1
Eye Irritation1

Reporter sex

5 reports
Female · 100%
Reports over time (by year) — tap or hover for the count & year
2022 2023 2024 2026 1 0
Most recent year is provisional (FAERS lags ~3 months).
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
50390-0111-00 You're viewing this 30 mL in 1 BOTTLE (50390-111-00) 2013-05-06 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 — Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured) ✓ Available
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The FDA registers it as 50390-111-00, 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: 50390-0111-00, written without dashes as 50390011100. 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 50390-0111-00, the first segment (50390) is the labeler code FDA assigned to Amway Corp; the middle segment (0111) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (00) identifies this exact package size and type. Together they name one specific package of one specific product.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Amway Corp. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Amway Corp 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 4 words ▾

Uses Helps prevent sunburn

⏱️ Dosage and Administration 95 words ▾

Directions For sunscreen use Apply liberally 15 minutes before sun exposure Use a water resistant sunscreen if swimming or sweating or washing Reapply at least every 2 hours 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 of 15 or higher and other sun protection measures including: Sun Protection Measures. limit time in the sun, especially from 10 a.m. – 2 p.m. wear long-sleeve shirts, pants, hats, and sunglasses Children under 6 months: ask a doctor

⚠️ Warnings 35 words ▾

Warnings For external use only. on broken or damaged skin. Do not use keep out of eyes. Rinse with water to remove. When using this product if rash occurs. Stop use and ask a doctor

📦 Storage and Handling 11 words ▾

Other information Protect this product from excessive heat and direct sun

🧪 Active Ingredient 11 words ▾

Active Ingredients Octinoxate 7.5% (W/W / P/P) Oxybenzone 0.5% (W/W P/P)

🧪 Inactive Ingredients 98 words ▾

Inactive Ingredients WATER/AQUA/EAU, CYCLOPENTASILOXANE, METHYL TRIMETHICONE, BUTYLENE GLYCOL, GLYCERIN, LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE, TALC, DIMETHICONE, TRIMETHYLOLPROPANE TRICAPRYLATE/TRICAPRATE, POLYGLYCERYL-6 POLYRICINOLEATE, HDI/ TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER, DIMETHICONE/PEG-10/15 CROSSPOLYMER, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, PHENOXYETHANOL, SODIUM CHLORIDE, SODIUM CITRATE, POLYGLYCERYL- 3 POLYDIMETHYLSILOXYETHYL DIMETHICONE, TRIETHOXYCAPRYLYLSILANE, ALUMINA, SORBITAN LAURATE, ALUMINUM HYDROXIDE, STEARIC ACID, METHYLPARABEN, SODIUM HYALURONATE, PROPYLPARABEN, FRAGRANCE/ PARFUM, HYDROXYETHYLCELLULOSE, ACETYL DIPEPTIDE-1 CETYL ESTER, ETHYLPARABEN, SILICA, IODOPROPYNYL BUTYLCARBAMATE, LECITHIN, CHLORELLA VULGARIS EXTRACT, GLYCINE SOJA (SOYBEAN) OIL, CERAMIDE-3, LIMNANTHES ALBA (MEADOWFOAM) SEED OIL, BETA-SITOSTEROL, PERILLA OCYMOIDES SEED OIL, SALVIA HISPANICA SEED OIL, OENOTHERA BIENNIS (EVENING PRIMROSE) OIL, TETRAHEXYLDECYL ASCORBATE.

MAY CONTAIN/PEUT CONTEINIR:TITANIUM DIOXIDE, IRON OXIDES, BISMUTH OXYCHLORIDE

🎯 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 ↗
← 50390-0108-30 · Amway 50390-0200-30 · Amway →
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.