Home NDC 87591-001 Bephor Reviving Suncream SPF50
Product NDC 87591-001
11-digit product format 875910001
Labeler code 87591
Product ID 87591-001_4c055b22-94ea-ff0d-e063-6394a90ab2ec
Type HUMAN OTC DRUG
Nonproprietary name Ethylhexyl Methoxycinnamate, Homosalate, Zinc Oxide
Dosage form LOTION
Route TOPICAL
Labeler Gyeongbuk Institute of IT Convergence Industry Technology
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-06-25
Substance HOMOSALATE; ZINC OXIDE; ETHYLHEXYL METHOXYCINNAMATE
Active strength 5; 12.5; 3.75 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 Bephor Reviving Suncream SPF50
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 5 g/50mL ZINC OXIDE 12.5 g/50mL ETHYLHEXYL METHOXYCINNAMATE 3.75 g/50mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination V06SV4M95S Internal UNII lookup SOI2LOH54Z Internal UNII lookup 4Y5P7MUD51 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 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 87591-001-02 87591000102 1 TUBE in 1 BOX (87591-001-02) / 50 mL in 1 TUBE (87591-001-01) 1 tube 2026-06-25 No No Current