Home NDC 76162-941 AVOBENZONE, HOMOSALATE, OCTISALATE
Product NDC 76162-941
11-digit product format 761620941
Labeler code 76162
Product ID 76162-941_58636012-7e2a-7206-e063-6394a90a83e9
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE, HOMOSALATE, OCTISALATE
Dosage form SPRAY
Route TOPICAL
Labeler Topco Associates LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-06
Substance AVOBENZONE; HOMOSALATE; OCTISALATE
Active strength 30; 100; 50 mg/g; mg/g; mg/g
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 AVOBENZONE, HOMOSALATE, OCTISALATE
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 30 mg/g HOMOSALATE 100 mg/g OCTISALATE 50 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination G63QQF2NOX Internal UNII lookup V06SV4M95S Internal UNII lookup 4X49Y0596W 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 76162-941-14 76162094114 156 g in 1 CAN (76162-941-14) 156 g 2026-08-06 No No Current