Aloe Cort

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: Aloe Cort
Generic name: HYDROCORTISONE
Manufacturer: Topiderm, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 789a6669-3320-4558-8d6f-ab255db50d8d
SPL ID: 5ddca73e-dfd3-446f-a0d2-3daadc9abddb
Version: 9
Effective date: 2019-09-17
Source export date: 2026-10-27
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/2026-10-27/b7a5e61d87a3b8f87f4c3ff7b526bfbf6baf84c840f565574c7d83d4083e2b38/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:47:00

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		Aloe Cort	openfda.brand_name
generic name		HYDROCORTISONE	openfda.generic_name
manufacturer name		Topiderm, Inc.	openfda.manufacturer_name
ndc	package	51326-108-57	openfda.package_ndc
ndc	product	51326-108	openfda.product_ndc
ndc11	package	51326010857	derived:openfda.package_ndc
rxcui		106258	openfda.rxcui
spl id		5ddca73e-dfd3-446f-a0d2-3daadc9abddb	id
spl set id		789a6669-3320-4558-8d6f-ab255db50d8d	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 the eyes. If condition worsens, or if symptoms persist for more than 7 days, or clear up and occur again within a few days, stop use of this product and consult a physician Do not use for treatment of diaper rash Keep out of reach of children. If swallowed, seek professional assistance or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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