FDA label cecc8791-8e76-7dde-e053-2a95a90a7944

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
7c602222-1480-6762-e053-2991aa0a4f9b
SPL ID
cecc8791-8e76-7dde-e053-2a95a90a7944
Version
4
Effective date
2021-10-20
Source export date
2026-09-28
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:58:43

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 Allergy Alert: if you are allergic to any ingredient of this product or chili peppers contact a doctor before use On wounds or to damaged skin With, or at same time as, other analgesic products With a heating pad 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 Stop use and ask a doctor if 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 If pregnant or breastfeeding consult a healthcare professional before use. 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.