FDA.reportPublic FDA data

Hydrocortisone

openFDA label record#

Cross-check layer: This is openFDA JSON-derived label data. Use the corresponding DailyMed SPL as the canonical label.

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

Brand name
Hydrocortisone
Generic name
HYDROCORTISONE
Manufacturer
J&A Digital Inc.
Product type
HUMAN OTC DRUG
SPL set ID
ff95a536-35b3-4006-b43c-cce359e86aa9
SPL ID
28ebcf7e-5bb5-dcdc-e063-6294a90abe86
Version
4
Effective date
2024-12-10
Source export date
2026-08-01
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/8ac060fefb6f4d67c41cc2c9e4330286ca93c48094c18386c11bf706a1d8bd34/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:27:24
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. Consult a doctor. Stop use and ask a doctor if condition worsens of lasts more than 7 days, or clears up and occurs again within a few days. you begin use of any other hydrocortisone product bleeding occurs Keep out of reach of children. If swallowed contact a Poison Control Center right away.