FDA label 0a478e25-0782-6851-e063-6394a90a588d

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
1635b177-e525-446a-8363-b0bc4bb83529
SPL ID
0a478e25-0782-6851-e063-6394a90a588d
Version
10
Effective date
2023-11-16
Source export date
2026-10-12
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:53:53

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 if you are a diabetic or have poor blood circulation, except under the advice and supervision of a doctor or podiatrist Do not use on irritated, infected or reddened skin genital warts and warts on the face moles, birthmarks and warts with hair growing from them mucous membranes such as nose, anus, genitals and lips Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away. Stop use and ask a doctor If discomforts persists see your doctor or podiatrist.

Reported adverse events (FAERS/openFDA)#

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