Alocane Anti-Itch

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: Alocane Anti-Itch
Generic name: HYDROCORTISONE 1%
Manufacturer: Quest Products, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 45252043-d41a-3cdd-e063-6394a90aa9e5
SPL ID: 4b235f6d-d684-e3a3-e063-6294a90a02fa
Version: 2
Effective date: 2026-02-18
Source export date: 2026-09-28
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/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:17:23

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 · 18 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Alocane Anti-Itch	openfda.brand_name
generic name		HYDROCORTISONE 1%	openfda.generic_name
manufacturer name		Quest Products, LLC	openfda.manufacturer_name
ndc	package	68229-411-03	openfda.package_ndc
ndc	package	68229-411-02	openfda.package_ndc
ndc	package	68229-411-01	openfda.package_ndc
ndc	package	68229-411-04	openfda.package_ndc
ndc	product	68229-411	openfda.product_ndc
ndc11	package	68229041101	derived:openfda.package_ndc
ndc11	package	68229041103	derived:openfda.package_ndc
ndc11	package	68229041102	derived:openfda.package_ndc
ndc11	package	68229041104	derived:openfda.package_ndc
rxcui		198706	openfda.rxcui
rxcui		2728413	openfda.rxcui
spl id		4b235f6d-d684-e3a3-e063-6294a90a02fa	id
spl set id		45252043-d41a-3cdd-e063-6394a90aa9e5	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 When using this product avoid contact with eyes Stop use and ask a doctor 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 do not begin use of any other hydrocortisone product unless you have consulted a doctor. Do not use for the treatment of diaper rash Do not use if you have vaginal discharge. Consult a doctor. Do not exceed the recommended daily dosage unless directed by a doctor. In case of bleeding, consult a doctor promptly. Do not put this product into the rectum by using fingers or any mechanical device or applicator. Kep out of reach of children If swallowed, get medical help or contact Poison Control Center reight away.

Reported adverse events (FAERS/openFDA)#

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