Home NDC 73492-291 1% Hydrocortisone Anti-itch
Product NDC 73492-291
11-digit product format 734920291
Labeler code 73492
Product ID 73492-291_57979a5b-49cc-3ede-e063-6394a90a3254
Type HUMAN OTC DRUG
Nonproprietary name 1% Hydrocortisone Anti-itch
Dosage form CREAM
Route TOPICAL
Labeler ALAINA HEALTHCARE PRIVATE LIMITED
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-07-20
Substance HYDROCORTISONE
Active strength 10 mg/g
Pharmacologic classes Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
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 1% Hydrocortisone Anti-itch
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HYDROCORTISONE 10 mg/g
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.
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 18 of 153 · 3,057 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 73492-291-28 73492029128 1 TUBE in 1 CARTON (73492-291-28) / 28 g in 1 TUBE 1 tube 2026-07-21 No No Current