Home NDC 68715-458 DD Cream
Product NDC 68715-458
11-digit product format 687150458
Labeler code 68715
Product ID 68715-458_414ce0da-4c4c-08c1-e063-6394a90aad77
Type HUMAN OTC DRUG
Nonproprietary name DD Cream
Dosage form CREAM
Route TOPICAL
Labeler DERMAdoctor, Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2014-11-26
Substance ZINC OXIDE; TITANIUM DIOXIDE
Active strength 12.05; 3.3 mg/100mL; mg/100mL
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 DD Cream
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 12.05 mg/100mL TITANIUM DIOXIDE 3.3 mg/100mL
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.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 68715-458-01 DD Cream 40 mL in 1 TUBE CREAM 40 3 68715-458-01 DD Cream 1 in 1 CARTON CREAM 1 3
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 68715-458-01 68715045801 1 TUBE in 1 CARTON (68715-458-01) / 40 mL in 1 TUBE 1 tube 2015-10-12 No No Current