Home NDC 87204-159-01 ONSART Mineral Sunscreen
Product NDC 87204-159
Requested package NDC 87204-159-01
11-digit product format 872040159
Labeler code 87204
Product ID 87204-159_48c9d08d-9a92-7df5-e063-6294a90a1c4a
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide 24%
Dosage form SPRAY
Route TOPICAL
Labeler Guangzhou Huixue Biotechnology Co., Ltd.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-01-15
Marketing end 2027-01-26
Substance ZINC OXIDE
Active strength 48 mg/200g
NDC exclude flag No
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 ONSART Mineral Sunscreen Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 48 mg/200g
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.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 87204-159-01 ONSART Mineral Sunscreen 200 g in 1 BOTTLE, PLASTIC SPRAY 200 1
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 87204-159-01 87204015901 200 g in 1 BOTTLE, PLASTIC (87204-159-01) 200 g 2026-01-15 2027-01-26 No No Historical