Home NDC 24208-001 PURPOSE
Product NDC 24208-001
11-digit product format 242080001
Labeler code 24208
Product ID 24208-001_22f5cdc2-86cc-7dfd-e063-6394a90a539d
Type HUMAN OTC DRUG
Nonproprietary name Octinoxate, Octisalate and Oxybenzone
Dosage form LOTION
Route TOPICAL
Labeler Bausch & Lomb Incorporated
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2013-10-07
Substance OCTINOXATE; OCTISALATE; OXYBENZONE
Active strength 7.5; 5; 3 g/100g; g/100g; g/100g
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 PURPOSE
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTINOXATE 7.5 g/100g OCTISALATE 5 g/100g OXYBENZONE 3 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4Y5P7MUD51 Internal UNII lookup 4X49Y0596W Internal UNII lookup 95OOS7VE0Y 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 24208-001-04 PURPOSE 113 g in 1 BOTTLE LOTION 113 3 24208-001-04 PURPOSE 1 in 1 CARTON LOTION 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 24208-001 PURPOSE (OCTINOXATE, OCTISALATE AND OXYBENZONE) LOTION [BAUSCH & LOMB INCORPORATED] 3 Current NDC, Legacy NDC, 2 package rows 20240927_a1e14135-b8da-4cee-8c5b-1893572f4de4.zip
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 6 of 25 · 494 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 24208-001-04 24208000104 1 BOTTLE in 1 CARTON (24208-001-04) / 113 g in 1 BOTTLE 1 bottle 2013-10-07 0000-00-00 No No Current