Home › NDC Lookup › Ingredients › Butyl Methoxydibenzoylmeth, Ethylhexyl S... › 82953-0046-03
SPF30 unseen sunscreen 01 butyl Methoxydibenzoylmeth, ethylhexyl salicylate, homosalate, octocrylene 3 g/100mL; 10 g/100mL; 10 g/100mL; 5 g/100mL Cream, 50 mL — NDC 82953-0046-03 package photo

SPF30 unseen sunscreen 01 butyl Methoxydibenzoylmeth, ethylhexyl salicylate, homosalate, octocrylene 3 g/100mL; 10 g/100mL; 10 g/100mL; 5 g/100mL Cream, 50 mL

by Cosmuses Cosmetics (Ningbo) Co., Ltd. · 50 mL in 1 TUBE (82953-046-03)
NDC 82953-0046-03
🏷️ FDA NDC (as labeled) 82953-046-03 billing pads the product segment with a zero
This package
Contains50 mL Pack sizes4 compare ↓
Also comes in: 10 ml 82953-0046-01 30 ml 82953-0046-02 60 ml 82953-0046-04
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) 82953-046-03
Product NDC 82953-046
11-digit billing NDC 82953004603
UNII G63QQF2NOX, V06SV4M95S, 5A68WGF6WM, 4X49Y0596W
Application # M020
SPL Set ID 398bb1f5-80ea-c589-e063-6294a90abefd
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-07-10
Route TOPICAL
Dosage form CREAM
Substance BUTYL METHOXYDIBENZOYLMETHANE; HOMOSALATE; OCTOCRYLENE; ETHYLHEXYL SALICYLATE
Why two NDCs? The FDA registers this code as 82953-046-03 — 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 → 82953-0046-03. 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 marketedJul 2025
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 an over-the-counter sunscreen cream applied to the skin to help protect against sun damage. It contains four ultraviolet light filters: butyl methoxydibenzoylmethane, ethylhexyl salicylate, homosalate, and octocrylene. These ingredients are commonly used together in sunscreen products to absorb and scatter both UVA and UVB rays. The product is formulated with an SPF rating of 30.

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 XLW9XG1719
    A waxy compound made from sucrose (sugar) and stearic acid. It acts as an emulsifier to blend water and oil ingredients, and helps create a smooth texture in the medicine.
  • 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 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 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 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 H1109Z9J4N
    A natural emulsifier derived from soybean oil. It helps mix oil and water-based ingredients together, ensuring even distribution of active ingredients throughout the medicine.
  • 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 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 5926LC4S7M
    Sucrose dilaurate is a synthetic compound made from sugar and lauric acid. It acts as an emulsifier and surfactant to help mix and stabilize ingredients that normally don't blend well together in medicines.
  • UNII 05Q7CD0E49
    A fatty acid derivative made from natural sugar and lauric acid. It acts as an emulsifier and solubilizer in medicines, helping mix water and oil-based ingredients together and improve how the body absorbs certain drugs.
  • UNII 3OSQ643ZK5
    Sucrose palmitate is a manufactured ingredient made by combining sugar with palmitic acid. It acts as an emulsifier and surfactant, helping oils and water mix together smoothly in liquid or semi-solid medicines.
  • UNII SZF3GPA9YV
    A synthetic ingredient made from sugar and fatty acids, used as an emulsifier to help blend oil and water-based components together in medications. It also improves texture and stability.
  • UNII 274KW0O50M
    Sucrose stearate is a compound made from sugar and stearic acid (a fatty substance). It works as an emulsifier and surfactant to help mix oils and water-based ingredients together in the medicine.
  • 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.

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

The official label also statesCaprylic/Capric Triglyceride, Glycerin, Water, Sucrose Polystearate, Sucrose Polylaurate, Sucrose Palmitate, Ethylhexylglycerin, Sucrose Dilaurate, Sucrose Distearate, Sucrose Stearate, Fragrance, Hydrogenated Lecithin, Ceramide NP, Sodium Hyaluronate.

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: 10 ml 30 ml 60 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
SPF30 unseen sunscreen 01 3 g/100mL; 10 g/100mL; 10 g/100mL; 5 g/100mLthis 82953-0046-03 Cosmuses 50 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

🏛️
2025
On the market since
Jul 2025
📍
2026
Currently FDA-listed
1 year 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
82953-0046-01 10 mL in 1 TUBE (82953-046-01) 2025-07-10 Active
82953-0046-02 30 mL in 1 TUBE (82953-046-02) 2025-07-10 Active
82953-0046-03 You're viewing this 50 mL in 1 TUBE (82953-046-03) 2025-07-10 Active
82953-0046-04 60 mL in 1 TUBE (82953-046-04) 2025-07-10 Active

You're viewing one of 4 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 82953-0046-03?
NDC 82953-0046-03 contains 50 mL — 50 ml in 1 tube.
What is the difference between NDC 82953-0046-03 and NDC 82953-0046-01?
Both are SPF30 unseen sunscreen 01 butyl Methoxydibenzoylmeth, ethylhexyl salicylate, homosalate, octocrylene 3 g/100mL; 10 g/100mL; 10 g/100mL; 5 g/100mL Cream — the drug itself is identical. NDC 82953-0046-03 is the 50 mL package, while NDC 82953-0046-01 is the 10 ml package.
What NDC number is used to bill for this package of SPF30 unseen sunscreen 01 butyl Methoxydibenzoylmeth, ethylhexyl salicylate, homosalate, octocrylene 3 g/100mL; 10 g/100mL; 10 g/100mL; 5 g/100mL Cream?
Bill NDC 82953-0046-03 — the 11-digit billing format is 82953004603. 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 ✓ 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 82953-046-03, 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: 82953-0046-03, written without dashes as 82953004603. 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 82953-0046-03, the first segment (82953) is the labeler code FDA assigned to Cosmuses Cosmetics (Ningbo) Co., Ltd.; the middle segment (0046) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (03) 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 3 other package presentations of this same product, including 10 ml (82953-0046-01), 30 ml (82953-0046-02), 60 ml (82953-0046-04). 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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 10 words ▾

Reapply as needed or after towel drying, swimming, or perspiring.

⏱️ Dosage and Administration 27 words ▾

Directions Apply liberally 15-20 minutes before sun exposure. Reapply as needed or after towel drying, swimming, or perspiring. Children under 6 months of age: ask a doctor

⚠️ Warnings 5 words ▾

Warnings For external use only.

🧪 Active Ingredient 12 words ▾

Active ingredients Butyl Methoxydibenzoylmethane 3% Ethylhexyl Salicylate 5% Homosalate 10% Octocrylene 10%

🧪 Inactive Ingredients 26 words ▾

Inactive ingredients Caprylic/Capric Triglyceride, Glycerin, Water, Sucrose Polystearate, Sucrose Polylaurate, Sucrose Palmitate, Ethylhexylglycerin, Sucrose Dilaurate, Sucrose Distearate, Sucrose Stearate, Fragrance, Hydrogenated Lecithin, Ceramide NP, Sodium Hyaluronate.

🎯 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 ↗
← 82953-0045-01 · Cosmuses 82953-0047-01 · 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.