Home NDC 49967-007 Maybelline New York Instant Age Rewind Eraser Treatment Makeup Broad Spectrum SPF 18 Sunscreen
Product NDC 49967-007
11-digit product format 499670007
Labeler code 49967
Product ID 49967-007_7df9995e-46d4-4308-8316-e55016fbc550
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 2010-01-01
Substance OCTINOXATE
Active strength 75 mg/mL
NDC exclude flag No
Listing certified through 2026-12-31
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 Maybelline New York Instant Age Rewind Eraser Treatment Makeup Broad Spectrum SPF 18 Sunscreen
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTINOXATE 75 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4Y5P7MUD51 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 49967-007-01 Maybelline New York Instant Age Rewind Eraser Treatment Makeup Broad Spectrum SPF 18 Sunscreen 20 mL in 1 BOTTLE LOTION 20 3
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49967-007 MAYBELLINE NEW YORK INSTANT AGE REWIND ERASER TREATMENT MAKEUP BROAD SPECTRUM SPF 18 SUNSCREEN (OCTINOXATE) LOTION [L'OREAL USA PRODUCTS INC] 3 Current NDC, Legacy NDC, 1 package rows 20231229_ea0609be-eaa9-4b63-9f07-e2cd974e01ba.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 162 of 353 · 7,049 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 49967-007-01 49967000701 20 mL in 1 BOTTLE (49967-007-01) 20 ml 2010-01-01 0000-00-00 No No Current