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 ACETATE
Manufacturer
JHK Inc dba American Safety & First Aid
Product type
HUMAN OTC DRUG
SPL set ID
64adc8d0-7ca4-4c1a-813f-f1df47e916f2
SPL ID
10a607b9-d690-40aa-b3d6-d2f5000a398b
Version
2
Effective date
2024-04-25
Source export date
2026-10-30
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-30/a3e33fe073aa0aa94eb690c6684c74434c63cebfbf7c5530205a2c3e957ecb8b/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run
20261102T182004Z
Imported at
2026-11-02 19:37:50
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 With any other hydrocortisone product unless you have consulted a doctor For the treatment of diaper rash, consult a doctor Stop use and ask a doctor if Condition worsens Symptoms persist for more than seven days Symptoms clear up and occur again within a few days 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.