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SLMD Avobenzone, Octinoxate, Octisalate, Oxybenzone 1.5 mg/g; 3.5 mg/g; 2.5 mg/g; 7.5 mg/g Cream — NDC 73318-7008-02 package photo

SLMD Avobenzone, Octinoxate, Octisalate, Oxybenzone 1.5 mg/g; 3.5 mg/g; 2.5 mg/g; 7.5 mg/g Cream

by Skin PS Brands · 1 TUBE in 1 CARTON (73318-7008-2) / 60 g in 1 TUBE
NDC 73318-7008-02
🏷️ FDA NDC (as labeled) 73318-7008-2 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) 73318-7008-2
Product NDC 73318-7008
11-digit billing NDC 73318700802
UNII 4X49Y0596W, 95OOS7VE0Y, G63QQF2NOX, 4Y5P7MUD51
UPC 0854977007032
Application # M020
SPL Set ID 1aa36c01-21b5-f06e-e063-6294a90a608f
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-06-11
Route TOPICAL
Dosage form CREAM
Substance OCTISALATE; OXYBENZONE; AVOBENZONE; OCTINOXATE
Why two NDCs? The FDA registers this code as 73318-7008-2 — 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 → 73318-7008-02. 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.

🏭 Manufacturer & labeler

LabelerSkin PS Brands
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code73318
First marketedJun 2024
Product typeHuman Otc Drug
Portfolio9 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?

SLMD Avobenzone, Octinoxate, Octisalate, Oxybenzone is a topical cream sunscreen marketed under FDA's OTC monograph rules. It contains four UV-filtering chemicals that work together to help protect skin from ultraviolet radiation. Avobenzone, octinoxate, octisalate, and oxybenzone are all commonly used as active ingredients in over-the-counter sunscreen products to absorb or reflect UV rays from the sun.

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 A7E6112E4N
    A form of vitamin E used as an antioxidant in medicines. It prevents oils and fats in the product from breaking down, helping maintain stability and shelf life.
  • UNII 4FRY3LJG0V
    A fungal protein component used as a binder and structural agent in some pharmaceutical formulations. It helps hold tablet ingredients together and may improve the stability of certain medicine preparations.
  • UNII 344S277G0Z
    Allantoin is a naturally derived compound that helps soften and soothe skin. In medicines, it works as a skin-conditioning agent and may help support wound healing and reduce irritation in topical formulations.
  • UNII 94ZLA3W45F
    Arginine is an amino acid used in medicines as a buffer and pH adjuster. It helps maintain the proper acidity level and stability of liquid formulations.
  • UNII Z54S26111B
    Ascorbyl linoleate is a compound combining vitamin C with linoleic acid, a fatty acid. It serves as an antioxidant in medicines to prevent degradation of active ingredients and maintain product stability during storage.
  • UNII 5SHP745C61
    A quaternary ammonium compound used as an antistatic agent and conditioning ingredient in solid dosage forms. It reduces static electricity buildup during manufacturing and helps improve the texture and flow of powders and granules in tablets or capsules.
  • UNII 2GXJ790US0
    A plant-derived oil from borage seeds, used as an emollient and skin-conditioning agent in topical formulations to help soften and smooth the product's texture on application.
  • UNII 9I2BJY2J17
    A plant extract from tea flowers used as a natural coloring agent and antioxidant in medicines. It helps maintain product stability and may provide a subtle color to the formulation.
  • 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 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 936JST6JCN
    Cetyl alcohol is a waxy, fatty substance derived from plant or animal sources. It acts as an emulsifier and thickener in medicines, helping blend oil and water components and giving products a smooth, creamy texture.
  • UNII 6A7N43E0OJ
    A natural oil from grapefruit peel used as a flavoring agent to improve taste and provide a citrus scent to the medicine.
  • UNII 4UG0316V9S
    A chemical compound used as an emulsifier and surfactant in topical medicines. It helps blend oil and water ingredients together and improves how the product spreads on skin or absorbs into it.
  • 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 7FLD91C86K
    Edetate disodium is a chemical compound that binds and removes certain metal ions. In medicines, it acts as a preservative and stabilizer by preventing metals like calcium from interfering with the product's shelf life and consistency.
  • UNII ANA2NCS6V1
    A natural oil derived from macadamia nuts, used as an emollient and conditioning agent. It helps soften the product's texture and improve how it spreads or absorbs on skin or mucous membranes.
  • 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 V663Q8TEFU
    A plant extract from witch hazel that acts as an astringent and skin-conditioning agent in topical medicines. It helps tighten tissues and is used for its traditional soothing properties in formulations.
  • UNII PG6M3969SG
    Lysophosphatidic acid is a lipid derived from natural fats. It acts as an emulsifier and penetration enhancer in medications, helping to improve absorption and mix oil and water-based ingredients together in formulations.
  • UNII AMR73HY95Q
    A synthetic peptide derived from amino acids. It functions as a skin-conditioning agent and emollient in topical formulations, helping soften and smooth the product's texture on application.
  • UNII PMA59A699X
    A synthetic peptide (short protein fragment) used as a thickener and film-former in topical formulations. It helps create texture, improve spreadability, and maintain product consistency on skin.
  • 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 832C4KF14X
    A synthetic oil derived from pentaerythritol and fatty acids. It acts as an emollient and solubilizer in formulations, helping dissolve active ingredients and improve texture and spreadability in topical or oral 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 MZQ63P0N0W
    A plant-derived emulsifier made from glycerin and castor oil. It helps mix oil and water ingredients together in formulations like creams and lotions, keeping them blended.
  • UNII SZ1T9D7ZKX
    A plant-derived oily substance made from glycerin and oleic acid. It works as an emulsifier and solubilizer in medicines, helping mix oily and watery ingredients together and keeping them blended throughout the product's shelf life.
  • UNII CAL22UVI4M
    A synthetic emulsifier derived from sorbitol and fatty acids. It helps mix oil and water-based ingredients together and improves the texture and stability of the medicine.
  • UNII 88R97D8U8A
    A synthetic liquid derived from propylene glycol and myristic acid. It functions as an emollient and solvent in topical formulations, helping to soften the skin and improve the texture and spreadability of the product.
  • UNII 61911N8D6W
    Retinyl linoleate is a derivative of vitamin A combined with linoleic acid, a natural fatty acid. It's used in medicines as an emollient and skin-conditioning agent to help soften and protect the skin.
  • UNII CR7307M3QZ
    Rosa canina fruit oil is a natural oil extracted from rosehip fruit. It's used in medicines as an emollient and skin-conditioning agent to help soften and smooth the product's texture or skin contact surface.
  • UNII 2YGO1190AP
    A plant-derived carbohydrate from yeast or fungi, chemically modified to carry sodium and carboxyl groups. It acts as a thickener, stabilizer, and binder in medications to improve texture, consistency, and shelf life.
  • UNII 1D1K0N0VVC
    A fat-soluble form of vitamin A used as a colorant and nutritional fortification ingredient. It gives products a yellow or orange tint and increases vitamin A content in the formula.
  • 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 14C97E680P
    Wheat germ oil is an oil extracted from wheat kernels. It's used in medicines as an emollient and lubricant to improve texture and help ingredients blend smoothly.

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

The official label also statesWater, Emulsifying Wax NF, Cetyl Alcohol, Glycerin, DEA-Cetyl Phosphate, Dimethicone, Behentrimonium Methosulfate, Cetearyl Alcohol, Myristol Pentapeptide-17, Myristol Pentapeptide-13, Ascorbyl Loneleate, Retinyl Linoleate, Lysophophatidic Acid, Penthonol, Allantoin, Arginine, Beta-Glucan, Sodium Carboxymethyl Beta-Glucan, Ethyl Macadamiate, Borago Officinail Seed OPil, Tiricum Vulgare (Wheat) Germ Oil, Tocopheryl Acetate, Retinyl Palmitate, Citrus Paradisi (Grapefruit) Fruit Extract, Camellia Sinensis Leaf Extract, Rosa Canina Fruit Extract, Hamamelis Virginiana (Witch Hazel) Extract, Polyglyceryl-3 Polyricinoleate, Polyglyceryl-5 Oleate, PPG-2 Myristyl Ether Propionate, Pentaerythrityl Tetracaprylate/Tetracaprate, Disodium EDTA, Caprylyl Glycol, Phenoxyethanol

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
Slmd 1.5 mg/g; 3.5 mg/g; 2.5 mg/g; 7.5 mg/gthis 73318-7008-02 Skin 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

🏛️
2024
On the market since
Jun 2024
📍
2026
Currently FDA-listed
2 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
73318-7008-02 You're viewing this 1 TUBE in 1 CARTON (73318-7008-2) / 60 g in 1 TUBE 2024-06-11 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 73318-7008-2, 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: 73318-7008-02, written without dashes as 73318700802. 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 73318-7008-02, the first segment (73318) is the labeler code FDA assigned to Skin PS Brands; the middle segment (7008) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (02) 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 Skin PS Brands. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Skin PS Brands 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 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 104 words ▾

Directions apply liberally and evenly 15 minutes before sun exposure. reapply at least every 2 hours use a water resistant sunscreen if swimming or sweating: immediately after towel drying 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 10 a.m. - 2 p.m. wear long-sleeved shirts, pants, hats and sunglasses

⚠️ Warnings 55 words ▾

Warnings For external use only. Do not use on damaged or broken skin. When using this product keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if rash occurs. Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 12 words ▾

Drug Facts Active Ingredient Avobenzone 2.5% Octinoxate 7.5% Octisalate 1.5% Oxybenzone 3.5%

🧪 Inactive Ingredients 81 words ▾

Inactive Ingredients Water, Emulsifying Wax NF, Cetyl Alcohol, Glycerin, DEA-Cetyl Phosphate, Dimethicone, Behentrimonium Methosulfate, Cetearyl Alcohol, Myristol Pentapeptide-17, Myristol Pentapeptide-13, Ascorbyl Loneleate, Retinyl Linoleate, Lysophophatidic Acid, Penthonol, Allantoin, Arginine, Beta-Glucan, Sodium Carboxymethyl Beta-Glucan, Ethyl Macadamiate, Borago Officinail Seed OPil, Tiricum Vulgare (Wheat) Germ Oil, Tocopheryl Acetate, Retinyl Palmitate, Citrus Paradisi (Grapefruit) Fruit Extract, Camellia Sinensis Leaf Extract, Rosa Canina Fruit Extract, Hamamelis Virginiana (Witch Hazel) Extract, Polyglyceryl-3 Polyricinoleate, Polyglyceryl-5 Oleate, PPG-2 Myristyl Ether Propionate, Pentaerythrityl Tetracaprylate/Tetracaprate, Disodium EDTA, Caprylyl Glycol, Phenoxyethanol

🎯 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 ↗
← 73318-7007-03 · Skin 73324-0001-01 · T. →
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.