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: 69d6645e-db3c-4dc0-a9a5-e2bc963e2f28
SPL ID: 3e4ef6bb-27cd-4a16-e063-6394a90a1e03
Version: 14
Effective date: 2025-09-08
Source export date: 2026-10-27
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/29a1aba6a935d72bab5474118c2ccf25cb52dfe8488fe1593c734ea6c04e3722/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 19:46:29

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 19 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Hydrocortisone	openfda.brand_name
generic name		HYDROCORTISONE	openfda.generic_name
manufacturer name		Unifirst First Aid Corporation	openfda.manufacturer_name
ndc	package	47682-397-73	openfda.package_ndc
ndc	package	47682-397-12	openfda.package_ndc
ndc	package	47682-397-99	openfda.package_ndc
ndc	package	47682-397-35	openfda.package_ndc
ndc	package	47682-397-71	openfda.package_ndc
ndc	product	47682-397	openfda.product_ndc
ndc11	package	47682039712	derived:openfda.package_ndc
ndc11	package	47682039771	derived:openfda.package_ndc
ndc11	package	47682039799	derived:openfda.package_ndc
ndc11	package	47682039773	derived:openfda.package_ndc
ndc11	package	47682039735	derived:openfda.package_ndc
rxcui		106258	openfda.rxcui
spl id		3e4ef6bb-27cd-4a16-e063-6394a90a1e03	id
spl set id		69d6645e-db3c-4dc0-a9a5-e2bc963e2f28	set_id
unii		WI4X0X7BPJ	openfda.unii

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 in eyes for feminine itching 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

Reported adverse events (FAERS/openFDA)#

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