FDA label 071fec28-fb86-9fc4-e063-6294a90a8b51

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
f418e0db-6baf-48fb-a023-1d1bf3a1b848
SPL ID
071fec28-fb86-9fc4-e063-6294a90a8b51
Version
5
Effective date
2023-10-07
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 05:31:41

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

Warning For external use only. Do not apply to wounds or damaged or irritated skin. Avoid contact with eyes and mucous membranes. If this occurs, wash the area thoroughly with water. You may experience a burning sensation when using this product which is normal and related to the way the product works. With regular use this sensation will disappear after several days. Do not apply immediately before or after activities such as strenuous exercise, bathing, swimming or sun bathing Do not tightly wrap or bandage the treated areas Do not apply heat or heating pad to the treated areas immediately before or after use Stop use and ask a doctor if Symptoms persist for more than seven days, discontinue use and consult a physician Rash/blistering occurs Difficulty breathing or swallowing occurs Severe burning pain persists Keep out the reach of children. If swallowed, get medical help or contact a poison control center immediately. If pregnant or breastfeeding, ask a physician before use.

Reported adverse events (FAERS/openFDA)#

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