FDA label f1b3aeb8-a1bb-a481-e053-2a95a90a19ad

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
0beabef1-13c2-426f-96a4-722973843c09
SPL ID
f1b3aeb8-a1bb-a481-e053-2a95a90a19ad
Version
4
Effective date
2023-01-07
Source export date
2026-09-28
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/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:49:29

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 • do not use for the treatment of diaper rash Consult a doctor: • before use if you have a vaginal discharge (for external feminine itching) • for external itching, do not exceed the recommended daily dosage or if bleeding occurs • If condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days When using this product: • avoid contact with eyes • do not put this product into rectum by using fingers or any mechanical device or applicator Do Not Use: • with any other Hydrocortisone product unless you have consulted a doctor.

Reported adverse events (FAERS/openFDA)#

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