Hydrocortisone 1% Anti-ItchCream

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 1% Anti-ItchCream
Generic name
HYDROCORTISONE
Manufacturer
Acme United Corporation
Product type
HUMAN OTC DRUG
SPL set ID
5425fc2b-4f25-3e64-e063-6394a90aff49
SPL ID
5425ff8d-cc9d-e5ef-e063-6294a90a585f
Version
1
Effective date
2026-06-13
Source export date
2026-09-28
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:26:24
Harmonized routes table
Harmonized routes
TOPICAL

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 Do not use 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. Consult a doctor. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

Reported adverse events (FAERS/openFDA)#

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