FDA label 1773ea79-e890-45cc-8e24-9d8b7b8664e0

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
22849dc6-3674-433d-8705-09cdbb314352
SPL ID
1773ea79-e890-45cc-8e24-9d8b7b8664e0
Version
6
Effective date
2012-02-01
Source export date
2026-09-28
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/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:21:56

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* use only as directed* do not bandage or use with a heating device* avoid contact with eyes and mucus membranes* do not apply to open wounds, broken or irritated skin* a transient warming sensation may occur upon application but generally disappears* do not expose the area treated with product to heat or sunlight.

Reported adverse events (FAERS/openFDA)#

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