Home NDC 87648-150 Bombee Honey Daily Glow Shield Sunscreen
Product NDC 87648-150
11-digit product format 876480150
Labeler code 87648
Product ID 87648-150_56112e06-d5e2-3fa3-e063-6294a90a04cb
Type HUMAN OTC DRUG
Nonproprietary name HOMOSALATE, OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE
Dosage form CREAM
Route TOPICAL
Labeler ABT ASIA Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-07-08
Substance TITANIUM DIOXIDE; HOMOSALATE; OCTOCRYLENE; OCTISALATE
Active strength .9; 3.65; 4.9; 2.45 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 Bombee Honey Daily Glow Shield Sunscreen
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE .9 g/50mL HOMOSALATE 3.65 g/50mL OCTOCRYLENE 4.9 g/50mL OCTISALATE 2.45 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.
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 87648-150-02 87648015002 1 BOTTLE in 1 BOX (87648-150-02) / 50 mL in 1 BOTTLE (87648-150-01) 1 bottle 2026-07-08 No No Current