Home NDC 85897-876 TINTED SUNSCREEN FOUNDATION
Product NDC 85897-876
11-digit product format 858970876
Labeler code 85897
Product ID 85897-876_4d37288a-be05-c62d-e063-6394a90a1171
Type HUMAN OTC DRUG
Nonproprietary name TINTED SUNSCREEN FOUNDATION
Dosage form LIQUID
Route CUTANEOUS
Labeler Guanghzou AiXin Biotech Co Ltd
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2025-07-08
Substance WATER; ZINC OXIDE
Active strength 35; 8 g/1; g/1
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base TINTED SUNSCREEN FOUNDATION
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 35 g/1 WATER 8 g/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup 059QF0KO0R Internal UNII lookup
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 85897-876-45 TINTED SUNSCREEN FOUNDATION 5 in 1 BOX LIQUID 5 2 85897-876-45 TINTED SUNSCREEN FOUNDATION 1 in 1 BOTTLE LIQUID 1 2
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 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 85897-876-45 85897087645 5 BOTTLE in 1 BOX (85897-876-45) / 1 LIQUID in 1 BOTTLE 5 bottle 2025-07-08 No No Current