Home NDC 82953-002 SUNSCREEN
Product NDC 82953-002
11-digit product format 829530002
Labeler code 82953
Product ID 82953-002_286c5fbb-74be-7de3-e063-6394a90a0973
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone,Homosalate,Octocrylene,Octisalate
Dosage form CREAM
Route TOPICAL
Labeler Cosmuses Cosmetics (Ningbo) Co., Ltd.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-09-26
Substance OCTOCRYLENE; HOMOSALATE; AVOBENZONE; OCTISALATE
Active strength 10; 10; 3; 5 g/100g; g/100g; g/100g; g/100g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base SUNSCREEN
Brand name suffix 01
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTOCRYLENE 10 g/100g HOMOSALATE 10 g/100g AVOBENZONE 3 g/100g OCTISALATE 5 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 82953-002-01 SUNSCREEN01 10 g in 1 BOTTLE, PLASTIC CREAM 10 4 82953-002-02 SUNSCREEN01 20 g in 1 BOTTLE, PLASTIC CREAM 20 4 82953-002-03 SUNSCREEN01 30 g in 1 BOTTLE, PLASTIC CREAM 30 4 82953-002-04 SUNSCREEN01 35 g in 1 BOTTLE, PLASTIC CREAM 35 4 82953-002-05 SUNSCREEN01 45 g in 1 BOTTLE, PLASTIC CREAM 45 4 82953-002-06 SUNSCREEN01 50 g in 1 BOTTLE, PLASTIC CREAM 50 4 82953-002-07 SUNSCREEN01 57 g in 1 BOTTLE, PLASTIC CREAM 57 4 82953-002-08 SUNSCREEN01 1.5 g in 1 BOTTLE, PLASTIC CREAM 1.5 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 82953-002 SUNSCREEN 01 (AVOBENZONE,HOMOSALATE,OCTOCRYLENE,OCTISALATE) CREAM [COSMUSES COSMETICS (NINGBO) CO., LTD.] 4 Current NDC, Legacy NDC, 8 package rows 20241206_e98c3b64-edcb-16c7-e053-2a95a90a8a0e.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 26 of 357 · 7,139 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 82953-002-01 82953000201 10 g in 1 BOTTLE, PLASTIC (82953-002-01) 10 g 2022-09-26 0000-00-00 No No Current 82953-002-02 82953000202 20 g in 1 BOTTLE, PLASTIC (82953-002-02) 20 g 2022-09-26 0000-00-00 No No Current 82953-002-03 82953000203 30 g in 1 BOTTLE, PLASTIC (82953-002-03) 30 g 2022-09-26 0000-00-00 No No Current 82953-002-04 82953000204 35 g in 1 BOTTLE, PLASTIC (82953-002-04) 35 g 2022-09-26 0000-00-00 No No Current 82953-002-05 82953000205 45 g in 1 BOTTLE, PLASTIC (82953-002-05) 45 g 2022-09-26 0000-00-00 No No Current 82953-002-06 82953000206 50 g in 1 BOTTLE, PLASTIC (82953-002-06) 50 g 2022-09-26 0000-00-00 No No Current 82953-002-07 82953000207 57 g in 1 BOTTLE, PLASTIC (82953-002-07) 57 g 2022-09-26 No No Current 82953-002-08 82953000208 1.5 g in 1 BOTTLE, PLASTIC (82953-002-08) 1.5 g 2022-09-26 No No Current