Home NDC 65582-839 Q Skin Science
Product NDC 65582-839
11-digit product format 655820839
Labeler code 65582
Product ID 65582-839_59e4c402-7586-7998-e063-6294a90a1440
Type HUMAN OTC DRUG
Nonproprietary name Sunscreen
Dosage form CREAM
Route TOPICAL
Labeler International Cosmeceuticals, Inc
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-08-01
Substance ZINC OXIDE; TITANIUM DIOXIDE
Active strength 4.01; 10.9 g/100g; g/100g
NDC exclude flag No
Listing certified through 2027-12-31
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 Q Skin Science
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 4.01 g/100g TITANIUM DIOXIDE 10.9 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup 15FIX9V2JP Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 Sample Exclude flag Status 65582-839-50 65582083950 50 g in 1 TUBE (65582-839-50) 50 g 2023-08-01 No No Current