Home NDC 69922-001 Marcelle CC Cream Complete Correction Sunscreen Broad Spectrum SPF 35
Product NDC 69922-001
11-digit product format 699220001
Labeler code 69922
Product ID 69922-001_d31dca97-f79f-4bf2-e053-2995a90ac4f6
Type HUMAN OTC DRUG
Nonproprietary name Octinoxate and Oxybenzone
Dosage form CREAM
Route TOPICAL
Labeler Groupe Marcelle Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2016-04-01
Substance OCTINOXATE; OXYBENZONE
Active strength 2.25; .9 g/30mL; g/30mL
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 Marcelle CC Cream Complete Correction Sunscreen Broad Spectrum SPF 35
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTINOXATE 2.25 g/30mL OXYBENZONE .9 g/30mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4Y5P7MUD51 Internal UNII lookup 95OOS7VE0Y Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69922-001-01 Marcelle CC Cream Complete Correction Sunscreen Broad Spectrum SPF 35 30 mL in 1 BOTTLE, PUMP CREAM 30 3 69922-001-01 Marcelle CC Cream Complete Correction Sunscreen Broad Spectrum SPF 35 1 in 1 CARTON CREAM 1 3 69922-001-02 Marcelle CC Cream Complete Correction Sunscreen Broad Spectrum SPF 35 7 mL in 1 TUBE CREAM 7 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69922-001 MARCELLE CC CREAM COMPLETE CORRECTION SUNSCREEN BROAD SPECTRUM SPF 35 (OCTINOXATE AND OXYBENZONE) CREAM [GROUPE MARCELLE INC.] 3 Current NDC, Legacy NDC, 3 package rows 20241004_c24ac3ad-b2e2-4381-bd80-a499da0e0670.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 26 of 357 · 7,139 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 69922-001-01 69922000101 1 BOTTLE, PUMP in 1 CARTON (69922-001-01) / 30 mL in 1 BOTTLE, PUMP 2016-04-01 0000-00-00 No No Current 69922-001-02 69922000102 7 mL in 1 TUBE (69922-001-02) 7 ml 2016-04-01 0000-00-00 No No Current