Home NDC 52000-022 Hydrocortisone Anti-Itch
Product NDC 52000-022
11-digit product format 520000022
Labeler code 52000
Product ID 52000-022_a27c1753-a558-4cf9-ba63-992d0c4cfde3
Type HUMAN OTC DRUG
Nonproprietary name Hydrocortisone
Dosage form CREAM
Route TOPICAL
Labeler Universal Distribution Center LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-12-09
Substance HYDROCORTISONE
Active strength .01 g/g
Pharmacologic classes Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 8 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 52000-022-37 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 52000-022-37 f5e01cc5f278…a2eaf40c39c3…2020-12-18 03:04 UTC · source 2020-12-17 excluded product product e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 52000-022-37 e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 52000-022-37 9bebd1f3094a…5416666fcb17…
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 Hydrocortisone Anti-Itch
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HYDROCORTISONE .01 g/g
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 52000-022-38 Hydrocortisone Anti-Itch 14 g in 1 TUBE CREAM 14 4 52000-022-39 Hydrocortisone Anti-Itch 1 in 1 BOX CREAM 1 4 52000-022-36 Hydrocortisone Anti-Itch 14 g in 1 TUBE CREAM 14 3 52000-022-37 Hydrocortisone Anti-Itch 1 in 1 BOX CREAM 1 3
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 52000-022 HYDROCORTISONE ANTI-ITCH (HYDROCORTISONE) CREAM [UNIVERSAL DISTRIBUTION CENTER LLC] 3 Current NDC, Legacy NDC, 2 package rows 20241212_d44ee37a-305e-4adc-be42-4928d6771655.zip 52000-022 HYDROCORTISONE ANTI-ITCH (HYDROCORTISONE) CREAM [UNIVERSAL DISTRIBUTION CENTER LLC] 3 Current NDC, Legacy NDC, 2 package rows 20241220_186afb11-06b6-4bfa-e063-6294a90aefc6.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 50 of 152 · 3,029 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 52000-022-36 52000002236 14 g in 1 TUBE 14 g Historical 52000-022-37 52000002237 1 TUBE in 1 BOX (52000-022-37) > 14 g in 1 TUBE (52000-022-36) 1 tube 2020-12-09 0000-00-00 No No Current 52000-022-38 52000002238 14 g in 1 TUBE 14 g Historical 52000-022-39 52000002239 1 TUBE in 1 BOX (52000-022-39) / 14 g in 1 TUBE (52000-022-38) 1 tube 2020-12-09 No No Current