FDA label 0e238099-20ab-47b0-9f95-86d252067194

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
5d2efce6-3cb4-4c86-b899-c1611a25384e
SPL ID
0e238099-20ab-47b0-9f95-86d252067194
Version
1
Effective date
2013-05-10
Source export date
2026-10-12
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:51:49

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 When using this product: Avoid contact with eyes, lips or mucous membranes DO NOT apply over deep or punctured wounds, infections or lacerations. Skin may become more sensitive to the sun, mild stinging, burning or peeling may occur. Use sunscreen or avoid exposure. If irritation occurs. Discontinue use immediately and consult physician for appropiate therapy. If pregnant or nursing consult your physician or pharmacist

Reported adverse events (FAERS/openFDA)#

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