FDA label fc5f2212-8ecc-e4c8-e053-6394a90a7483

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)

SPL set ID
acc79e55-fa58-2915-e053-2a95a90a0101
SPL ID
fc5f2212-8ecc-e4c8-e053-6394a90a7483
Version
3
Effective date
2023-05-23
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:39:06

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 2 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.

warnings

When using this product Avoid contact with the 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 the 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.

Reported adverse events (FAERS/openFDA)#

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