Home NDC 69729-269 Quatriderm Anti-itch
Product NDC 69729-269
11-digit product format 697290269
Labeler code 69729
Product ID 69729-269_0bb8304b-0ea3-8c48-e063-6394a90a3a15
Type HUMAN OTC DRUG
Nonproprietary name Hydrocortisone
Dosage form CREAM
Route TOPICAL
Labeler OPMX LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-03-03
Substance HYDROCORTISONE
Active strength 1 g/100g
Pharmacologic classes Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
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 Quatriderm Anti-itch
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HYDROCORTISONE 1 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination WI4X0X7BPJ Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 106258 Internal RxNorm 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 69729-269-53 Quatriderm Anti-itch 1 in 1 CARTON CREAM 1 8 69729-269-53 Quatriderm Anti-itch 56 g in 1 TUBE CREAM 56 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69729-269 QUATRIDERM ANTI-ITCH (HYDROCORTISONE) CREAM [OPMX LLC] 8 Current NDC, Legacy NDC, 2 package rows 20231207_83e59e10-9878-e5c2-e053-2a91aa0af25e.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 8 of 156 · 3,115 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 69729-269-53 69729026953 1 TUBE in 1 CARTON (69729-269-53) / 56 g in 1 TUBE 1 tube 2023-06-01 0000-00-00 No No Current