CVS Health 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
CVS Health Hydrocortisone Anti Itch
Generic name
HYDROCORTISONE
Manufacturer
CVS Health
Product type
HUMAN OTC DRUG
SPL set ID
546a1b8a-8254-432a-85c4-38ebee5ad568
SPL ID
95d465a5-3d68-4693-a2ea-1e312d2500a0
Version
2
Effective date
2024-08-07
Source export date
2026-09-28
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/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:53:24
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 begin the use of any other hydrocortisone product unless you have consulted a doctor. for external genital, feminine and anal itching do not exceed the recommended daily dosage unless directed by a doctor. In case of bleeding, stop use, consult 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 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. Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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