FDA label fc79b514-fc63-5a5d-e053-6294a90a03c6

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
95bad924-4ff2-003b-e053-2995a90a200c
SPL ID
fc79b514-fc63-5a5d-e053-6294a90a03c6
Version
6
Effective date
2023-05-24
Source export date
2026-10-12
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:38:37

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. Ask a doctor if condition worsens, deep puncture wounds, animal bites, or serious burns. Stop use and ask a doctor if the condition worsens, or if symptoms persist for more than 7days or clear up and occur again within a few days. Do not begin to use any other hydrocortisone product unless you have consulted a doctor. If Pregnant or breast-feeding, ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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