Home NDC 87283-006 SUNSCREEN GLOWING
Product NDC 87283-006
11-digit product format 872830006
Labeler code 87283
Product ID 87283-006_47df0de5-012b-c896-e063-6394a90a9cef
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE ,OCTISALATE ,OCTOCRYLENE , HOMOSALATE
Dosage form LOTION
Route TOPICAL
Labeler Aopline Biotechnology (Guangzhou) Co., Ltd.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-01-08
Substance OCTOCRYLENE; OCTISALATE; HOMOSALATE; AVOBENZONE
Active strength 3.5; 2.5; 4.5; 1.5 g/50mL; g/50mL; g/50mL; g/50mL
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 SUNSCREEN GLOWING
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTOCRYLENE 3.5 g/50mL OCTISALATE 2.5 g/50mL HOMOSALATE 4.5 g/50mL AVOBENZONE 1.5 g/50mL
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 87283-006-01 SUNSCREEN GLOWING 60 mL in 1 BOTTLE LOTION 60 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 Sample Exclude flag Status 87283-006-01 87283000601 60 mL in 1 BOTTLE (87283-006-01) 60 ml 2026-01-08 No No Current