FDA label cdc69602-de28-1e35-e053-2995a90a2baa

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
cae03130-ecb9-b01c-e053-2995a90aa46b
SPL ID
cdc69602-de28-1e35-e053-2995a90a2baa
Version
2
Effective date
2021-10-07
Source export date
2026-09-28
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:09:47

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 damaged skin with a heating pad if you are allergic to capsicum or chili peppers When using this product avoid contact with the eyes and mucus membranes a transient burning sensation may occur upon application but generally disappears in a few days do not bandage tightly do not apply heat to treated area Stop use and ask a doctor if condition worsens or if symptoms last more than 7 day or clear up and occur again within a few days. redness or irritation develop. a severe burning sensation occurs. 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.