FDA.reportPublic FDA data

FDA label 9d91ffac-cb8b-4b94-8107-57f39732dd7b

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
fbf3bea8-556d-4f98-9e99-a0a2b7931af7
SPL ID
9d91ffac-cb8b-4b94-8107-57f39732dd7b
Version
3
Effective date
2013-09-03
Source export date
2026-11-06
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/245ea1c0d730b312e4410f082201cbe2cb4d1936fa2918316b6ea631293cbeba/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 08:07:12

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 On an area that is infected and/or bleeding Chafing due to deep puncture wounds, animal bites and/or serious burns When using this product Keep out of eyes and mouth Stop use an ask a doctor if Certain persons can develop allergic reactions to ingredients in this product. If the symptom being treated does not subside or if redness, Irritation, swelling, pain or other symptoms develop or increase, discontinue use and consult a doctor

Reported adverse events (FAERS/openFDA)#

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