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SUNSCREEN 01 Avobenzone,Homosalate,Octocrylene,Octisalate 10 g/100mL; 10 g/100mL; 3 g/100mL; 5 g/100mL Cream, 15 mL

by Cosmuses Cosmetics (Ningbo) Co., Ltd. · 15 mL in 1 BOTTLE, PLASTIC (82953-017-01)
NDC 82953-0017-01
🏷️ FDA NDC (as labeled) 82953-017-01 billing pads the product segment with a zero
This package
Contains15 mL Pack sizes13 compare ↓
Also comes in: 1.5 ml 82953-0017-13 20 ml 82953-0017-11 30 ml 82953-0017-02 35 ml 82953-0017-05 45 ml 82953-0017-12 50 ml 82953-0017-06 60 ml 82953-0017-03 75 ml 82953-0017-04 90 ml 82953-0017-10 120 ml 82953-0017-07 240 ml 82953-0017-08 300 ml 82953-0017-09
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) 82953-017-01
Product NDC 82953-017
11-digit billing NDC 82953001701
UNII 5A68WGF6WM, V06SV4M95S, G63QQF2NOX, 4X49Y0596W
Application # M020
SPL Set ID 19a7dc68-6384-3783-e063-6394a90ac839
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-05-30
Route TOPICAL
Dosage form CREAM
Substance OCTOCRYLENE; HOMOSALATE; AVOBENZONE; OCTISALATE
Why two NDCs? The FDA registers this code as 82953-017-01 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 82953-0017-01. 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

LabelerCosmuses Cosmetics (Ningbo) Co., Ltd.
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code82953
First marketedMay 2024
Product typeHuman Otc Drug
Portfolio66 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 cream sunscreen formulated with four UV-filtering ingredients: avobenzone, homosalate, octisalate, and octocrylene. These active ingredients function as chemical sunscreens, each absorbing ultraviolet radiation to help reduce skin exposure to UV rays. This is an over-the-counter monograph product, meaning it is marketed under the FDA's established rules for sunscreen drugs rather than through individual application review. The cream is applied directly to the skin as a sun protection product.

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 1P9D0Z171K
    BHT is a synthetic antioxidant that prevents fats and oils in medicines from breaking down and becoming rancid. It helps keep the product stable and effective during storage.
  • UNII E4F12ROE70
    A refined mineral oil derived from crude petroleum containing 13 to 14 carbon chains. It acts as a solvent, emollient, and carrier in topical formulations to help dissolve active ingredients and improve product texture and spreadability.
  • UNII 5KLY4IOG20
    A synthetic detergent made from cetyl alcohol and ethylene oxide. It acts as an emulsifier to help mix oil and water-based ingredients, and as a solubilizer to keep active ingredients dissolved 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 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 5EM498GW35
    A mixture of aromatic compounds used to add pleasant smell to the medicine. Fragrance helps mask unpleasant tastes or odors, making the medication easier to take.
  • 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 FCZ5MH785I
    A waxy substance made from glycerin and stearic acid. It works as an emulsifier to help mix oil and water ingredients together, and as a thickener to give the medicine its proper texture and consistency.
  • UNII 0RE8K4LNJS
    Isopropyl myristate is an oily liquid made from coconut or palm oil. It's used in medicines as an emollient and penetration enhancer to help the medicine absorb through skin or improve spreadability in topical products.
  • UNII Z95S6G8201
    A synthetic surfactant derived from lauryl alcohol and ethylene oxide. It helps dissolve and mix oily and watery ingredients in liquid formulations, and may improve how the medicine spreads or is absorbed.
  • 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 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 RHA9LWJ494
    A synthetic polymer formed by linking acrylamide molecules together. It functions as a binder and thickener in medicines, helping hold ingredients together and adjust the product's texture and consistency.
  • 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 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 2ZA36H0S2V
    Beeswax is a natural wax produced by honeybees. In medicines, it works as a coating agent and thickener to control how fast the drug dissolves and improve the product's texture and appearance.

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

The official label also statesAqua, Glycerin, Isopropyl Myristate, Cetearyl Alcohol, Glyceryl Stearate, Ceteth-25, Beeswax, Phenoxyethanol, Fragrance, Methylparaben, Polyacrylamide, C13-14 Isoparaffin, Laureth-7, Propylparaben, Disodium EDTA, BHT

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.
Try another pack size: 1.5 ml 20 ml 30 ml 35 ml 45 ml 50 ml 60 ml 75 ml 90 ml 120 ml 240 ml 300 ml
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
REEF SAFE Unscented SPF Mineral Sunscreen 01 10 g/100mL; 10 g/100mL; 3 g/100mL; 5 g/100mL 82953-0027-01 Cosmuses 45 ml — — FDA listed —
Sun ,Bug Handsfree 01 10 g/100mL; 10 g/100mL; 3 g/100mL; 5 g/100mL 82953-0010-01 Cosmuses 10 ml — — FDA listed —
Sunscreen 01 10 g/100mL; 10 g/100mL; 3 g/100mL; 5 g/100mL 82953-0023-01 Cosmuses 15 ml — — FDA listed —
Sunscreen 01 10 g/100mL; 10 g/100mL; 3 g/100mL; 5 g/100mLthis 82953-0017-01 Cosmuses 15 ml — — 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
May 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.

🔬 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 SUNSCREEN 01 (this brand).

Top reported reactions

Rash13
Acne10
Dry Skin9
Erythema9
Sunburn9
Malignant Melanoma8
Headache7

Age at onset

Child1
Adult9
Elderly11

Reporter sex

141 reports
Male · 36%
Female · 64%

Serious outcomes

Hospitalization22
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 14 1
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
82953-0017-01 You're viewing this 15 mL in 1 BOTTLE, PLASTIC (82953-017-01) 2024-05-30 Active
82953-0017-02 30 mL in 1 BOTTLE, PLASTIC (82953-017-02) 2024-05-30 Active
82953-0017-03 60 mL in 1 BOTTLE, PLASTIC (82953-017-03) 2024-05-30 Active
82953-0017-04 75 mL in 1 BOTTLE, PLASTIC (82953-017-04) 2024-05-30 Active
82953-0017-05 35 mL in 1 BOTTLE, PLASTIC (82953-017-05) 2024-05-30 Active
82953-0017-06 50 mL in 1 BOTTLE, PLASTIC (82953-017-06) 2024-05-30 Active
82953-0017-07 120 mL in 1 BOTTLE, PLASTIC (82953-017-07) 2024-05-30 Active
82953-0017-08 240 mL in 1 BOTTLE, PLASTIC (82953-017-08) 2024-05-30 Active
82953-0017-09 300 mL in 1 BOTTLE, PLASTIC (82953-017-09) 2024-05-30 Active
82953-0017-10 90 mL in 1 BOTTLE, PLASTIC (82953-017-10) 2024-05-30 Active
82953-0017-11 20 mL in 1 BOTTLE, PLASTIC (82953-017-11) 2024-05-30 Active
82953-0017-12 45 mL in 1 BOTTLE, PLASTIC (82953-017-12) 2024-05-30 Active
82953-0017-13 1.5 mL in 1 POUCH (82953-017-13) 2024-05-30 Active

Pack size FAQ

What quantity is in NDC 82953-0017-01?
NDC 82953-0017-01 contains 15 mL — 15 ml in 1 bottle, plastic.
What is the difference between NDC 82953-0017-01 and NDC 82953-0017-13?
Both are SUNSCREEN 01 Avobenzone,Homosalate,Octocrylene,Octisalate 10 g/100mL; 10 g/100mL; 3 g/100mL; 5 g/100mL Cream — the drug itself is identical. NDC 82953-0017-01 is the 15 mL package, while NDC 82953-0017-13 is the 1.5 ml package.
What NDC number is used to bill for this package of SUNSCREEN 01 Avobenzone,Homosalate,Octocrylene,Octisalate 10 g/100mL; 10 g/100mL; 3 g/100mL; 5 g/100mL Cream?
Bill NDC 82953-0017-01 — the 11-digit billing format is 82953001701. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 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 82953-017-01, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 82953-0017-01, written without dashes as 82953001701. 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 82953-0017-01, the first segment (82953) is the labeler code FDA assigned to Cosmuses Cosmetics (Ningbo) Co., Ltd.; the middle segment (0017) 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 Cosmuses Cosmetics (Ningbo) Co., Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 12 other package presentations of this same product, including 1.5 ml (82953-0017-13), 20 ml (82953-0017-11), 30 ml (82953-0017-02). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
Cosmuses Cosmetics (Ningbo) Co., Ltd. is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.

📄 FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 28 words ▾

Uses Helps prevent sunburn If used as directed with other sun protection measures (see Directions), decreased the risk of skin cancer and early skin aging caused by sun.

⏱️ Dosage and Administration 86 words ▾

Directions apply liberally 15minutes before sun exposure reapply: after 80 minutes of swimming or sweating immediate after towel drying at least every 2 hours Sun Protection Measures Spending time increases your risk of skin cancer and early skin aging. To decreases this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: limit time in the sun, especially from 10a.m.- 2p.m. wear long-sleeve shirts, pants, hats and sunglasses children under 6 months Ask a doctor

⚠️ Warnings 5 words ▾

Warnings For external use only

📦 Storage and Handling 11 words ▾

Other information Protect this product from excessive heat and direct sun

🧪 Active Ingredient 10 words ▾

Active ingredients Avobenzone 3% Homosalate 10% Octocrylene 10% Octisalate 5%

🧪 Inactive Ingredients 23 words ▾

Inactive ingredients Aqua, Glycerin, Isopropyl Myristate, Cetearyl Alcohol, Glyceryl Stearate, Ceteth-25, Beeswax, Phenoxyethanol, Fragrance, Methylparaben, Polyacrylamide, C13-14 Isoparaffin, Laureth-7, Propylparaben, Disodium EDTA, BHT

🎯 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 ↗
← 82953-0016-01 · Cosmuses 82953-0018-01 · Cosmuses →
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.