Home NDC 22700-030 Covergirl Outlast Extreme Wear 3-in-1 Foundation 24 HR Full Coverage SPF 18 Octinoxate Sunscreen Liquid Foundation
Product NDC 22700-030
11-digit product format 227000030
Labeler code 22700
Product ID 22700-030_258e8f05-295f-8e32-e063-6294a90a7548
Type HUMAN OTC DRUG
Nonproprietary name OCTINOXATE
Dosage form EMULSION
Route TOPICAL
Labeler Noxell Corporation
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-12-01
Substance OCTINOXATE
Active strength 30 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 Covergirl Outlast Extreme Wear 3-in-1 Foundation 24 HR Full Coverage SPF 18 Octinoxate Sunscreen Liquid Foundation
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTINOXATE 30 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 22700-030-01 Covergirl Outlast Extreme Wear 3-in-1 Foundation 24 HR Full Coverage SPF 18 Octinoxate Sunscreen Liquid Foundation 1 in 1 CARTON EMULSION 1 1 22700-030-01 Covergirl Outlast Extreme Wear 3-in-1 Foundation 24 HR Full Coverage SPF 18 Octinoxate Sunscreen Liquid Foundation 30 mL in 1 BOTTLE EMULSION 30 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 22700-030 COVERGIRL OUTLAST EXTREME WEAR 3-IN-1 FOUNDATION 24 HR FULL COVERAGE SPF 18 OCTINOXATE SUNSCREEN LIQUID FOUNDATION (OCTINOXATE) EMULSION [NOXELL CORPORATION] 1 Current NDC, 2 package rows 20241123_258e8f05-295e-8e32-e063-6294a90a7548.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 242 of 353 · 7,049 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 22700-030-01 22700003001 1 BOTTLE in 1 CARTON (22700-030-01) / 30 mL in 1 BOTTLE 1 bottle 2021-12-01 No No Current