FDA label 0723d972-7a66-7a2c-e063-6394a90a93f2

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
82b55fdf-979e-4f8b-a70b-9817319556c1
SPL ID
0723d972-7a66-7a2c-e063-6394a90a93f2
Version
4
Effective date
2023-10-07
Source export date
2026-09-28
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/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:14:14

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 externa l use on l y. Avoid contact with eyes and mucous membranes. Do not bandage tight l y or cover treated areas. Do not use with heating pad. Do not app l y to open wounds or damaged skin. A mi l d burning sensation may occur. I f severe burning sensation occurs, discontinue use immediate l y. I f Symptoms persist for more than seven days, discontinue use and consu l t physician. Keep out of reach of children. I f swallowed, consult physician. If pregnant or breast feeding, contact physician prior to use.

Reported adverse events (FAERS/openFDA)#

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