FDA label 0e0f2899-5ea1-48a7-8e17-edea95ca737d

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
ae7273be-30ec-4c3b-ad2c-91073f667228
SPL ID
0e0f2899-5ea1-48a7-8e17-edea95ca737d
Version
4
Effective date
2019-02-11
Source export date
2026-10-12
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:30:47

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 and cautions

Only for external use Do not use on open wounds, cuts, damaged or infected skin as well as in the eyes, mouth, genitals or any other mucus membranes. Consult your physician: if pain is persistent or worsens or if using any other topical pain products. Call poison control if swallowed. If contact with eyes occurs, rinse eyes thoroughly with cold water. If a rash develops discontinue use and consult a physician. Use in pregnancy or nursing mother: No studies have been done on animals or humans.

Reported adverse events (FAERS/openFDA)#

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