FDA label 08f52343-b275-3c16-e063-6294a90af9b3

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
7d439082-06a2-4864-9669-b8dbdc7afa24
SPL ID
08f52343-b275-3c16-e063-6294a90af9b3
Version
2
Effective date
2023-10-30
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 08:07:59

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 FLAMMABLE. Keep away from heat, flame or sparks. This product is for external use only. For use on hands only. Do not use in or near the eyes. In case of eye contact, rinse thoroughly with water. Do not use on babies less than 2 months of age. Do not use on open wounds. Discontinue use if irritation or redness occurs. If condition persists for more than 72 hours, consult a doctor. Keep out of reach of children. If swallowed, seek medical advice or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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