FDA label 90cda10a-d624-db5e-e053-2995a90ac8e4

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
7fc2bf51-be32-cd1d-e053-2991aa0af519
SPL ID
90cda10a-d624-db5e-e053-2995a90ac8e4
Version
3
Effective date
2019-08-23
Source export date
2026-09-28
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:21:26

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 On wounds or to damaged skin With, or at same time as, other analgesic products Allergy Alert: if you are allergic to any ingredients of this product or chili peppers contact a doctor before use If pregnant or breastfeeding consult a healthcare professional before use When using this product You may experience a burning sensation which is normal and related to the way the product works. With regular use, this sensation generally diminishes. Do not use immediately before or after activities such as swimming, showering, sunbathing or intense exercise. Use only as directed Avoid contact with eyes and mucous membranes or rashes Ask a doctor before use if your condition worsens, symptoms persist more than 7 days or clear up and occur again within a few days rash, itching or excessive skin irritation develops 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.