Home NDC 87545-002 Mineral sunscreen
Product NDC 87545-002
11-digit product format 875450002
Labeler code 87545
Product ID 87545-002_59713657-a7f0-1aee-e063-6394a90a326e
Type HUMAN OTC DRUG
Nonproprietary name Mineral sunscreen
Dosage form LOTION
Route CUTANEOUS
Labeler Guangzhou Origin Beauty Cosmetics Co., Ltd.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-20
Substance ZINC OXIDE
Active strength 10 g/50g
NDC exclude flag No
Listing certified through 2027-12-31
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 Mineral sunscreen
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 10 g/50g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 162 of 353 · 7,049 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87545-002-01 87545000201 50 g in 1 BOTTLE, PUMP (87545-002-01) 50 g 2026-08-20 No No Current