Hydrocortisone

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
Hydrocortisone
Generic name
HYDROCORTISONE
Manufacturer
Unifirst First Aid Corporation
Product type
HUMAN OTC DRUG
SPL set ID
e90df2e5-2ef4-47dd-bd74-be9cea6d9d85
SPL ID
3e4cb58c-fe23-ca13-e063-6394a90a7244
Version
18
Effective date
2025-09-08
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:38:47
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only Do not use for the treatment of diaper rash with anyother Hydrocortisone product unless you have consulted adoctor if you have vaginal discharge, consulkt a doctor Stop use and ask a doctor if condition worsens or lasts more than 7 days, or clears and occurs again within a few days you begin use of any other Hydrocortisone product unless you have consulted a doctor bleeding occurs Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.