FDA.reportPublic FDA data

FDA label 499cae2f-13a0-45ec-af9c-aab2e35e4139

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
c68a65f0-fd01-4e1d-b6a3-7ac6952d2dfc
SPL ID
499cae2f-13a0-45ec-af9c-aab2e35e4139
Version
2
Effective date
2015-05-06
Source export date
2026-09-28
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:30:24

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 Do not use -other than as directed -with a heating pad (may blister skin) -on children under 12 years of age When using this product -avoid contact with the eyes or mucus membranes -do not apply to wounds or damaged skin -do not bandage tightly Stop use and ask a doctor if -skin redness or excessive irritation of the skin develops -condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days

Reported adverse events (FAERS/openFDA)#

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