FDA label f1b26eb5-bf86-1d24-e053-2a95a90a2f15

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: cfcf4c9b-e362-43cb-8446-c1aa67833a9e
SPL ID: f1b26eb5-bf86-1d24-e053-2a95a90a2f15
Version: 4
Effective date: 2023-01-07
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:29:50

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 2 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
spl id		f1b26eb5-bf86-1d24-e053-2a95a90a2f15	id
spl set id		cfcf4c9b-e362-43cb-8446-c1aa67833a9e	set_id

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

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 symptoms persist 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 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.