FDA.reportPublic FDA data

FDA label 471663b8-4afe-48c9-8ae8-0837c0b2ff2a

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
a970185c-c633-4d58-b593-b3f7cd289b94
SPL ID
471663b8-4afe-48c9-8ae8-0837c0b2ff2a
Version
1
Effective date
2021-06-29
Source export date
2026-11-06
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/db89d5ebfc3e02f44e8769334d799cd3436b05f779823ab00297f1f800c89ddf/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:30:48

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 Flammable: • keep away from fire or flame • contents under pressure • do not puncture or incinerate container • do not expose to temperatures above 120 F Do not use: • in or near muccous membrances • on serious burns • on deep puncture wounds • for a prolonged period of time • on a large portion of the body Stop use and ask a doctor if : • redness, swelling, or irritation occurs • infection occurs • condition persists or worsens • symptoms persist for more than 7 days.

Reported adverse events (FAERS/openFDA)#

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