FDA label b4481093-0eeb-4f58-b72d-f1dadf543d22

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
3c861266-3f46-4881-8b4e-1c43b27f4c07
SPL ID
b4481093-0eeb-4f58-b72d-f1dadf543d22
Version
1
Effective date
2009-11-23
Source export date
2026-10-12
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:35:42

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. Avoid contact with eyes and mucus membranes. Do not use on open wounds, damaged or irritated skin. Do not bandage tightly. A transient burning sensation may occur upon initial application, but usually disappears in a few days. If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again, with in a few days, discontinue use and consult a health professional. Do not use if shrink sleeve is broken or missing. Do not use if adverse effects occur. FLAMMABLE: Keep away from heat or flame. If you are pregnant or breast feeding, consult with a health professional prior to use. If swallowed, get medical assistance or contact a Poison Control Center Immediately. KEEP OUT OF REACH OF CHILDREN.

Reported adverse events (FAERS/openFDA)#

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