FDA label 8c122ff5-0f4c-4591-95f8-303e17075439

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
b38e1d36-e164-4b29-ac93-aaa009ef0844
SPL ID
8c122ff5-0f4c-4591-95f8-303e17075439
Version
1
Effective date
2022-03-17
Source export date
2026-09-28
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:28:12

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 if you are allergic to any of the active ingredients or inactive ingredients in this product. When using this product avoid contact with eyes and mouth do not use on wounds or irritated or damaged skin use only as directed do not apply tight wraps or bandages to treated areas do not apply heat to treated areas immediately before or after use Stop use and ask a doctor if symptoms persist more than 3 days or worsen symptoms clear up and then reoccur within a few days Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away.

Reported adverse events (FAERS/openFDA)#

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