Maximum Strength Hydrocortisone 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
Maximum Strength Hydrocortisone Anti-itch
Generic name
HYDROCORTISONE 1%
Manufacturer
Target Corporation
Product type
HUMAN OTC DRUG
SPL set ID
4ff39cb8-3a20-4fe7-9829-1e882a484668
SPL ID
b627e4d4-8fbe-4bbf-b399-ba2e37f173c7
Version
2
Effective date
2024-01-17
Source export date
2026-10-27
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-27/be847f9aea8d80a2cb7e9771acd1143be084664192ecf8f5be8ac1024116f4f0/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run
20261027T193451Z
Imported at
2026-10-27 20:12:25
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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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. for external genital itching if you have a vaginal discharge, consult a doctor. When using this product avoid contact with eyes do not use more than directed unless told ot do so by a doctor do not put this product into the rectum by using fingers or any mechanical device or applicator. Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and do not begin use of any other hydrocortisone product unless directed by a doctor. rectal bleeding occurs

Reported adverse events (FAERS/openFDA)#

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