Home NDC 85897-374 BODY / FACE SUNSCREEN SUN
Product NDC 85897-374
11-digit product format 858970374
Labeler code 85897
Product ID 85897-374_4d372a4d-ba8f-b8e4-e063-6294a90ae9d8
Type HUMAN OTC DRUG
Nonproprietary name BODY / FACE SUNSCREEN SUN
Dosage form CREAM, AUGMENTED
Route CUTANEOUS
Labeler Guanghzou AiXin Biotech Co., Ltd
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2025-07-03
Substance HOMOSALATE; OCTINOXATE
Active strength 7.5; 7.5 g/1; g/1
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 BODY / FACE SUNSCREEN SUN
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 7.5 g/1 OCTINOXATE 7.5 g/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination V06SV4M95S Internal UNII lookup 4Y5P7MUD51 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 85897-374-01 BODY / FACE SUNSCREEN SUN 5 in 1 BOX CREAM, AUGMENTED 5 2 85897-374-01 BODY / FACE SUNSCREEN SUN 1 in 1 BAG CREAM, AUGMENTED 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 85897-374-01 85897037401 5 BAG in 1 BOX (85897-374-01) / 1 CREAM, AUGMENTED in 1 BAG 5 bag 2025-07-08 No No Current