Home NDC 49967-202 MAYBELLINE NEW YORK INSTANT AGE REWIND ERASER TREATMENT MAKEUP OCTINOXATE BROAD SPECTRUM SPF 20 SUNSCREEN PLUS PROVITAMIN B5
Product NDC 49967-202
11-digit product format 499670202
Labeler code 49967
Product ID 49967-202_e4c50d8c-3ab1-4281-bd1a-34e90549ac30
Type HUMAN OTC DRUG
Nonproprietary name Octinoxate
Dosage form LOTION
Route TOPICAL
Labeler L'Oreal USA Products Inc
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-01-14
Substance OCTINOXATE
Active strength 75 mg/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base MAYBELLINE NEW YORK INSTANT AGE REWIND ERASER TREATMENT MAKEUP OCTINOXATE BROAD SPECTRUM SPF 20 SUNSCREEN PLUS PROVITAMIN B5
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTINOXATE 75 mg/mL
Harmonized Identifiers# Field, Values table Field Values Unii 4Y5P7MUD51
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 49967-202-01 MAYBELLINE NEW YORK INSTANT AGE REWIND ERASER TREATMENT MAKEUP OCTINOXATE BROAD SPECTRUM SPF 20 SUNSCREEN PLUS PROVITAMIN B5 20 mL in 1 BOTTLE LOTION 20 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49967-202 MAYBELLINE NEW YORK INSTANT AGE REWIND ERASER TREATMENT MAKEUP OCTINOXATE BROAD SPECTRUM SPF 20 SUNSCREEN PLUS PROVITAMIN B5 (OCTINOXATE) LOTION [L'OREAL USA PRODUCTS INC] 1 Current NDC, 1 package rows 20240629_12ec5a93-8c24-4ac9-94df-910dd8137e00.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 49967-202-01 49967020201 20 mL in 1 BOTTLE (49967-202-01) 20 ml 2024-01-14 No No Historical