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Solar Moisturizer SPF 30 Octinoxate, Oxybenzone, Octisalate, Avobenzone, Octocrylene 5 mg/g; 7.5 mg/g; 6 mg/g; 2 mg/g; 1.5 mg/g Cream, 1 tube — NDC 62742-4078-02 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Solar Moisturizer SPF 30 Octinoxate, Oxybenzone, Octisalate, Avobenzone, Octocrylene 5 mg/g; 7.5 mg/g; 6 mg/g; 2 mg/g; 1.5 mg/g Cream, 1 tube — NDC 62742-4078-2 (Billing 62742-4078-02)

by Allure Labs, LLC · 1 TUBE in 1 CARTON / 56.7 g in 1 TUBE

This is a package of 1 tube of Solar Moisturizer SPF 30 Octinoxate, Oxybenzone, Octisalate, Avobenzone, Octocrylene 5 mg/g; 7.5 mg/g; 6 mg/g; 2 mg/g; 1.5 mg/g Cream from Allure Labs, LLC, marketed since Oct 2019 and currently FDA-listed. It is this product's only package size.

NDC 62742-4078-02
🏷️ FDA NDC (as labeled) 62742-4078-2 billing pads the package segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed 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

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 62742-4078-2
Product NDC 62742-4078
11-digit billing NDC 62742407802
UNII 4X49Y0596W, 4Y5P7MUD51, 95OOS7VE0Y, G63QQF2NOX, 5A68WGF6WM
Application # M020
SPL Set ID ef4d54bf-25f5-4261-9d3d-c42b0d892275
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2019-10-15
Route TOPICAL
Dosage form CREAM
Substance OCTISALATE; OCTINOXATE; OXYBENZONE; AVOBENZONE; OCTOCRYLENE
Why two NDCs? The FDA registers this code as 62742-4078-2 — 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 → 62742-4078-02. 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.

Clinical

🧪 What is this product?

Solar Moisturizer SPF 30 is a topical cream marketed as an over-the-counter sunscreen product under FDA's OTC monograph rules. It contains five UV-filtering ingredients (avobenzone, octinoxate, octisalate, octocrylene, and oxybenzone) that are typically used together to absorb and scatter ultraviolet radiation from the sun. This combination of chemical sunscreen agents is commonly formulated in moisturizing creams intended for daily skin protection from sun exposure.

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.

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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
62742-4078-02 You're viewing this Main listing 1 TUBE in 1 CARTON / 56.7 g in 1 TUBE 2019-10-15 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Solar Moisturizer SPF 30 5 mg/g; 7.5 mg/g; 6 mg/g; 2 mg/g; 1.5 mg/gthis 62742-4078-02 Allure 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

🏛️
2019
On the market since
Oct 2019
📍
2026
Currently FDA-listed
7 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.

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 A9EJ3J61HQ
    A synthetic liquid derived from benzoic acid and long-chain alcohols. It functions as a solvent and penetration enhancer in topical formulations, helping active ingredients dissolve and absorb into the skin.
  • UNII ZY81Z83H0X
    Aloe vera leaf is a plant extract derived from the aloe plant. It is used in medicines as a natural moisturizer and skin-soothing agent in topical formulations.
  • UNII AI3L60HQ81
    A plant-derived substance from the model plant Arabidopsis thaliana, used as a natural binder or thickening agent to help hold the medicine together and improve its texture and stability.
  • UNII 3M5V3D1X36
    A plant extract from bearberry leaves, used in traditional medicine formulations. It may function as a natural flavoring agent or botanical additive in some preparations.
  • UNII JDR81QW9ZQ
    A plant material derived from mugwort, used as a filler or bulking agent in herbal formulations. It helps provide volume and structure to the medicine.
  • 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 QN83US2B0N
    Ascorbyl palmitate is a fat-soluble form of vitamin C used as an antioxidant in medicines. It prevents oils and fats in the product from breaking down and becoming less stable over time.
  • UNII 8SKN0B0MIM
    Benzoic acid is a naturally occurring organic acid used as a preservative in medicines and foods. It helps prevent bacterial and fungal growth to extend shelf life and maintain product stability.
  • UNII LKG8494WBH
    Benzyl alcohol is a clear liquid used as a preservative and solvent in medicines. It helps prevent bacterial and fungal growth and dissolves other ingredients to create uniform liquid formulations.
  • UNII WAO5MNK9TU
    Benzyl salicylate is a fragrant chemical compound used as a flavor and scent ingredient in medicines. It helps mask unpleasant tastes or odors in liquid or oral formulations.
  • 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 F9H6L20VOH
    Butyl cyanoacetate is a synthetic chemical compound used as a binder and adhesive agent in solid pharmaceutical formulations. It helps hold tablet or capsule ingredients together and improves product stability.
  • 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 EXY4496LWD
    A plant-derived ingredient from the pods of the Caesalpinia spinosa tree, native to South America. It's used as a natural thickener, binder, and source of fiber in formulations.
  • UNII 00YIU5438U
    Caprylyl glycol is a clear liquid derived from coconut oil. In medicines, it acts as a humectant to retain moisture, a preservative booster to prevent microbial growth, and a solvent to help dissolve or mix other ingredients.
  • UNII 0A5MM307FC
    A synthetic polymer that absorbs water and forms a thick, gel-like substance. In medicines, it works as a thickener and stabilizer to improve texture and help ingredients stay mixed together in creams, gels, and lotions.
  • UNII 59TL3WG5CO
    A synthetic polymer made by crosslinking acrylic acid with allyl sucrose. It thickens liquids, forms gels, and helps control how fast the medicine is released in your body.
  • UNII 7M867G6T1U
    Centella asiatica is a plant extract used in medicines as a skin-conditioning or soothing ingredient. It helps maintain product stability and may support skin comfort in topical formulations.
  • UNII 2968PHW8QP
    A weak organic acid derived from citrus fruits or made through fermentation. It works as a buffer to control pH, a preservative to extend shelf life, and a flavoring agent in medications.
  • 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 XHK3U310BA
    Cyclohexasiloxane is a silicon-based liquid that acts as a solvent and conditioning agent in medicines. It helps dissolve or carry other ingredients and improves how the product spreads or feels on the skin.
  • UNII EG8ODI0780
    Darutoside is a plant-derived compound used as a natural binder and film-former in medications. It helps hold tablet ingredients together and may coat capsules or tablets for controlled release.
  • UNII QI7G114Y98
    Echinacea purpurea is a dried plant extract from the purple coneflower. It's included in some formulations as a botanical ingredient to support the product's intended benefits, though it serves no structural role like binding or coating.
  • UNII 8NLQ36F6MM
    Edetate disodium anhydrous is a chemical compound that binds to metal ions in a medicine. It's used as a stabilizer to prevent unwanted chemical reactions and help keep the drug product effective during storage.
  • 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 3T8H1794QW
    Eugenol is a natural oil extracted from clove and other plants. It's used in medicines as a flavoring agent and to provide a mild anesthetic effect in topical products, particularly in dental formulations.
  • 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 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 W2ZU1RY8B0
    A plant extract from green tea leaves. It's used as an antioxidant ingredient to help preserve the medicine and maintain its stability during storage.
  • UNII 4P26HG1S5W
    A plant extract from sunflower sprouts used in formulations as an antioxidant and preservative to help maintain product stability and prevent degradation of active ingredients.
  • UNII KEH0A3F75J
    Hexylene glycol is a clear liquid alcohol used as a solvent and preservative in medicines. It helps dissolve other ingredients and keeps the product stable during storage.
  • 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 71ES77LGJC
    A natural extract from kiwi fruit used as a flavor and color agent in medicines. It adds taste appeal and may contribute a light color to the formulation.
  • UNII 15E7C67EE8
    A natural seaweed extract used as a thickener and gelling agent in medicines. It helps create the right texture and consistency in liquid or semi-solid formulations.
  • UNII EX0F4CZ66H
    A synthetic polymer made from lauryl methacrylate and glycol dimethacrylate monomers. Used as a film-coating agent to protect tablets and control how quickly the medicine dissolves in the digestive system.
  • UNII 1DI56QDM62
    A natural fatty substance from soybeans that helps mix oil and water-based ingredients together. It acts as an emulsifier and lubricant in medicines to improve texture and help the product break down properly in your body.
  • 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 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 LV6L29Z6AX
    A naturally occurring bacterium used as a preservative in some medications and cosmetics. It helps prevent microbial growth and extends product shelf life.
  • UNII 57P5O8083D
    A plant-derived ingredient from Mitracarpus hirtus used as a natural binder or filler to help hold tablet or capsule ingredients together and maintain product structure.
  • UNII X8725R883T
    A synthetic oily liquid derived from branched carboxylic acids, used as an emollient and skin-conditioning agent in topical formulations. It helps soften and smooth the product's texture while improving how it spreads on skin.
  • UNII KK181SM5JG
    A synthetic peptide derived from amino acids. In medications and cosmetic formulations, it functions as an active conditioning agent to help maintain skin texture and firmness in topical products.
  • UNII HIE492ZZ3T
    Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
  • UNII B697894SGQ
    Polyethylene glycol 400 is a clear, thick liquid made from petroleum-derived polymers. It acts as a solvent and humectant in medicines, helping dissolve active ingredients and retain moisture in the formulation.
  • UNII ZCD6009IUF
    A plant-derived ingredient from knotweed used as a natural filler and binding agent. It helps hold the medicine's ingredients together and add bulk to tablets or capsules.
  • UNII 7T1F30V5YH
    A synthetic emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together and keeps them from separating in liquid formulations.
  • UNII 1VPU26JZZ4
    Potassium sorbate is a salt derived from sorbic acid, a naturally occurring preservative. It prevents growth of mold, yeast, and some bacteria, extending the medicine's shelf life.
  • UNII 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • UNII OJ245FE5EU
    Sodium benzoate is a salt derived from benzoic acid, a preservative. It's added to medicines to prevent growth of bacteria, fungi, and other microorganisms that could spoil the product.
  • UNII TU7HW0W0QT
    A salt derived from lactic acid, sodium lactate acts as a buffer and pH stabilizer in medicines. It helps maintain the product's acidity level and can also serve as a humectant to retain moisture.
  • UNII 4VON5FNS3C
    Sodium metabisulfite is a preservative derived from sulfur compounds. It prevents microbial growth and oxidation in medicines, helping extend shelf life and maintain product stability.
  • UNII 06XEA2VD56
    Sorbitan oleate is an emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together and keeps them from separating in the medicine.
  • UNII S8S8451A4O
    Teprenone is a plant-derived alcohol used as a protective and healing agent in oral medications. It helps soothe and coat the stomach lining in certain gastrointestinal formulations.
  • 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 9O3K93S3TK
    Trolamine is an alkaline compound used as a pH buffer and emulsifier in medicines. It helps neutralize acids, stabilize formulations, and enable mixing of oil and water-based ingredients.
  • UNII EJ27X76M46
    Ubidecarenone is a naturally occurring compound found in cells that helps produce energy. In medicines, it acts as an antioxidant and may help stabilize the product while supporting cellular function in the body.
  • 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.
  • UNII 3NY3SM6B8U
    A microorganism used as a natural source of B vitamins and proteins. In medications, yeast serves as a nutrient supplement and may help with tablet binding or act as a filler to give the product proper form and stability.

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

The official label also statesInactive Ingredients: Water (Aqua), C12-15 Alkyl Benzoate, Butylene Glycol, Octyldodecyl Neopentanoate, Caprylic/Capric Triglyceride, Glycerin, Aloe Barbadensis Leaf Juice, Bis(Cyano Butylacetate) Anthracenediylidene, Disodium EDTA, Sorbitan Oleate, Ubiquinone, Teprenone, Carbomer, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Sodium Hyaluronate, Yeast Polysaccharides, Camellia Sinensis Leaf Extract, Actinidia Chinensis (Kiwi) Fruit Extract, Laminaria Digitata Extract, Artemisia Vulgaris Extract, Echinacea Purpurea Extract, Centella Asiatica Extract, Cyclopentasiloxane, Cyclohexasiloxane, Lauryl Methacrylate/Glycol Dimethacrylate Crosspolymer, Triethanolamine, PEG-8, Tocopherol, Ascorbyl Palmitate, Ascorbic Acid, Citric Acid, Polysorbate 20, Palmitoyl Pentapeptide-4, Darutoside, Arctostaphylos Uva Ursi Leaf Extract, Mitracarpus Scaber Extract, Plankton Extract, Lecithin, Micrococcus Lysate, Arabidopsis Thaliana Extract, Polygonum Aviculare Extract, Caesalpinia Spinosa Fruit Pod Extract, Helianthus Annuus (Sunflower) Sprout Extract, Propylene Glycol, Phenoxyethanol, Caprylyl Glycol, Ethylhexylglycerin, Hexylene Glycol, Potassium Sorbate, Sodium Benzoate, Sodium Metabisulfite, Sodium Lactate, Biotin, Xanthan Gum, Benzoic Acid, Fragrance (or) Parfum, Benzyl Alcohol, Benzyl Salicylate, Geraniol, Linalool, Eugenol

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.

Manufacturer & labeler

LabelerAllure Labs, LLC
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code62742
First marketedOct 2019
Product typeHuman Otc Drug
Portfolio3 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.

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 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 11 words ▾

Uses - This product is suited for broad spectrum UV Protection.

⏱️ Dosage and Administration 24 words ▾

Directions - Apply using fingertips 20-30 minutes before sun exposure. Gentely massage into face and neck. Reapply as needed. Discontinue use if irritation develops.

⚠️ Warnings 6 words ▾

Warnings - For external use only.

🧪 Active Ingredient 17 words ▾

Active Ingredients: Octinoxate - 7.5% Oxybenzone - 6.0% Octisalate - 5.0% Avobenzone - 2.0% Octocrylene - 1.5%

🧪 Inactive Ingredients 151 words ▾

Inactive Ingredients: Water (Aqua), C12-15 Alkyl Benzoate, Butylene Glycol, Octyldodecyl Neopentanoate, Caprylic/Capric Triglyceride, Glycerin , Aloe Barbadensis Leaf Juice , Bis(Cyano Butylacetate) Anthracenediylidene, Disodium EDTA, Sorbitan Oleate, Ubiquinone, Teprenone, Carbomer, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Sodium Hyaluronate, Yeast Polysaccharides, Camellia Sinensis Leaf Extract, Actinidia Chinensis (Kiwi) Fruit Extract, Laminaria Digitata Extract, Artemisia Vulgaris Extract, Echinacea Purpurea Extract, Centella Asiatica Extract , Cyclopentasiloxane, Cyclohexasiloxane, Lauryl Methacrylate/Glycol Dimethacrylate Crosspolymer, Triethanolamine , PEG-8, Tocopherol , Ascorbyl Palmitate , Ascorbic Acid , Citric Acid, Polysorbate 20, Palmitoyl Pentapeptide-4, Darutoside, Arctostaphylos Uva Ursi Leaf Extract , Mitracarpus Scaber Extract, Plankton Extract , Lecithin , Micrococcus Lysate, Arabidopsis Thaliana Extract , Polygonum Aviculare Extract, Caesalpinia Spinosa Fruit Pod Extract, Helianthus Annuus (Sunflower) Sprout Extract, Propylene Glycol, Phenoxyethanol, Caprylyl Glycol , Ethylhexylglycerin , Hexylene Glycol, Potassium Sorbate, Sodium Benzoate , Sodium Metabisulfite, Sodium Lactate, Biotin, Xanthan Gum, Benzoic Acid, Fragrance (or) Parfum, Benzyl Alcohol, Benzyl Salicylate, Geraniol, Linalool, Eugenol

🎯 Purpose 2 words ▾

Purpose: Sunscreen

📄 When Using This Product 22 words ▾

When using this product - Keep out of eyes. If contact occurs, rinse with water. Discontinue use if irritation or redness occurs.

📄 Stop Use and Ask a Doctor If 12 words ▾

Stop use and ask a doctor - If severe skin irritation develops.

📄 Keep Out of Reach of Children 19 words ▾

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

📄 Package Label / Principal Display Panel 15 words ▾

Manufactured for DermaQuest®, Inc. Hayward, CA 94544 1272 GK, NL Made in USA dermaquestinc.com IMGDQISMSPF30

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

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 form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
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 Allure Labs, LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Allure Labs, LLC is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.
← 62742-4077-01 · Allure 62742-4091-01 · ALLURE →
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.