Home NDC 75742-070 American Red Cross Anti-Itch
Product NDC 75742-070
11-digit product format 757420070
Labeler code 75742
Product ID 75742-070_41b8cb00-a04f-52f0-e063-6294a90aabf7
Type HUMAN OTC DRUG
Nonproprietary name Hydrocortisone 1.0%(w/w)
Dosage form SPRAY
Route TOPICAL
Labeler Zhejiang Guoyao Jingyue Aerosol Co., Ltd.
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-10-22
Substance HYDROCORTISONE
Active strength 1 g/100g
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 American Red Cross Anti-Itch
Listing expiration 2027-12-31 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 317564 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 75742-070-01 American Red Cross Anti-Itch 141 g in 1 BOTTLE, SPRAY SPRAY 141 1
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 28 of 68 · 1,357 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 75742-070-01 75742007001 141 g in 1 BOTTLE, SPRAY (75742-070-01) 141 g 2025-10-22 No No Current