Home NDC 82637-9455 Anti-Itch Vulva Cream 1 Hydrocortisone Acetate
Product NDC 82637-9455
11-digit product format 826379455
Labeler code 82637
Product ID 82637-9455_1ea12af8-cc63-6bfa-e063-6294a90a3302
Type HUMAN OTC DRUG
Nonproprietary name HYDROCORTISONE ACETATE
Dosage form CREAM
Route TOPICAL
Labeler The Honey Pot Company LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-03-01
Substance HYDROCORTISONE ACETATE
Active strength 10 mg/mL
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 Anti-Itch Vulva Cream 1 Hydrocortisone Acetate
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HYDROCORTISONE ACETATE 10 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3X7931PO74 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1039349 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 82637-9455-1 Anti-Itch Vulva Cream 1 Hydrocortisone Acetate 30 mL in 1 TUBE CREAM 30 3 82637-9455-1 Anti-Itch Vulva Cream 1 Hydrocortisone Acetate 1 in 1 CARTON CREAM 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 82637-9455 ANTI-ITCH VULVA CREAM 1 HYDROCORTISONE ACETATE (HYDROCORTISONE ACETATE) CREAM [THE HONEY POT COMPANY LLC] 3 Current NDC, Legacy NDC, 2 package rows 20240802_6f32b536-6ebf-49a8-abb6-2a1daae2f6d7.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 18 of 153 · 3,057 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 82637-9455-1 82637945501 1 TUBE in 1 CARTON (82637-9455-1) / 30 mL in 1 TUBE 1 tube 2022-03-01 0000-00-00 No No Current