FDA.reportPublic FDA data

FDA label 308335e3-71b6-4dd9-8495-d02b28b4caa6

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
d76beba5-c0b9-4016-afbe-592b0268fce7
SPL ID
308335e3-71b6-4dd9-8495-d02b28b4caa6
Version
1
Effective date
2015-08-28
Source export date
2026-10-12
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/7928c8e8c6256620071a8b7e5b93eb8dfa543649c08d17a01ea02251012ba58c/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:25:33

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 Discontinue use and consult a Physician if a rash or other adverse reaction occurs, or if symptoms worsen or persist for more than 7 days Children under 12 – Ask your doctor Avoid contact with eyes or mucus membranes If Pregnant or breast feeding, ask a physician before use Do not use with other topical products Do not use on open wounds If swallowed, seek professional help and contact Poison Control immediately Flammable Keep away from fire or flame

Reported adverse events (FAERS/openFDA)#

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