Home NDC 66820-0500 DECORTE AQ ABSOLUTE TREATMENT AWAKENING PROTECTIVE DAY
Product NDC 66820-0500
11-digit product format 668200500
Labeler code 66820
Product ID 66820-0500_46a18880-2cb4-cf89-e063-6394a90afb0e
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE, OCTINOXATE, OCTISALATE
Dosage form CREAM
Route TOPICAL
Labeler KOS� America, Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-05-16
Substance AVOBENZONE; OCTINOXATE; OCTISALATE
Active strength 30; 74.945; 10 mg/mL; mg/mL; 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 DECORTE AQ ABSOLUTE TREATMENT AWAKENING PROTECTIVE DAY
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 30 mg/mL OCTINOXATE 74.945 mg/mL OCTISALATE 10 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination G63QQF2NOX Internal UNII lookup 4Y5P7MUD51 Internal UNII lookup 4X49Y0596W 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 66820-0500-1 DECORTE AQ ABSOLUTE TREATMENT AWAKENING PROTECTIVE DAY 45 mL in 1 CYLINDER CREAM 45 2 66820-0500-1 DECORTE AQ ABSOLUTE TREATMENT AWAKENING PROTECTIVE DAY 1 in 1 CARTON CREAM 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 66820-0500 DECORTE AQ ABSOLUTE TREATMENT AWAKENING PROTECTIVE DAY (AVOBENZONE, OCTINOXATE, OCTISALATE) CREAM [KOSE AMERICA, INC.] 1 Current NDC, 2 package rows 20240517_81352963-36ec-4099-af51-3498d89f3077.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 354 · 7,077 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 66820-0500-1 66820050001 1 CYLINDER in 1 CARTON (66820-0500-1) / 45 mL in 1 CYLINDER 1 cylinder 2024-05-16 No No Current