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: Medrock Pharmacy LLC
Product type: HUMAN OTC DRUG
SPL set ID: 43e00e17-1a48-43db-9589-834568917bbf
SPL ID: 4b12aca8-f8aa-b413-e063-6294a90a0359
Version: 2
Effective date: 2026-02-17
Source export date: 2026-10-12
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:13:17

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 · 11 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		Medrock Pharmacy LLC	openfda.manufacturer_name
ndc	package	85402-001-01	openfda.package_ndc
ndc	product	85402-001	openfda.product_ndc
ndc11	package	85402000101	derived:openfda.package_ndc
rxcui		106258	openfda.rxcui
spl id		4b12aca8-f8aa-b413-e063-6294a90a0359	id
spl set id		43e00e17-1a48-43db-9589-834568917bbf	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 Avoid contact with eyes Stop use and ask a physician: if condition worsens or symptoms persist for 7 days or clears up and occurs again within a few days, discontinue use of this product and consult a physician Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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