FDA label d53fdd9a-6553-3573-e053-2995a90abeb0

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
fc79795f-25ce-4d06-88f6-5b1e4bf39815
SPL ID
d53fdd9a-6553-3573-e053-2995a90abeb0
Version
1
Effective date
2022-01-10
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 06:09:43

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 When using this product use only as directed consult your doctor before use if using any medications or supplements that contain any of these same ingredients do not bandage tightly do not use with heating pad avoid contact with eyes and mucous membranes do not apply to wounds, damaged, broken or irritated skin do not use at the same time as other topical analgesics Stop use and ask a doctor if condition worsens redness persists, spreads or becomes tender symptoms last more than 7 days or clear up and occur again within a few days you experience burning swelling or blistering where applied If pregnant or breast-feeding, ask 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.