FDA label 2b2b2e5d-ad74-4d36-ac5a-615a027bc5cc

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
5b4e7f72-8845-492a-afab-30f2d4556384
SPL ID
2b2b2e5d-ad74-4d36-ac5a-615a027bc5cc
Version
1
Effective date
2013-10-24
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:51:01

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 Keep out of reach of children. For esternal use only, use only as directed. Donot apply to wound or broken skin. If redness present discontinue and consult a doctor. Do not bandage tightly or use a heating pad. If the condition persists for more than 5 days, discontinue use and consult a doctor. Avoid contact with eyes and other mucous membranes. If you are pregnant or nursing a baby, seek the advice of a healthcare professional before using this product.

Reported adverse events (FAERS/openFDA)#

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