FDA label 4baddbc0-c919-477c-8b1a-0f005ec55810

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
3f6feec5-2019-4fe6-b2b9-fd1c04d9a1f1
SPL ID
4baddbc0-c919-477c-8b1a-0f005ec55810
Version
4
Effective date
2026-07-23
Source export date
2026-10-12
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:56:31

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 Rare cases of serious burns have been reported with products of this type Don't bandage tightly or use with a heating pad Avoid contact with eyes or mucous membranes Don't apply to wounds or damaged skin Do not use at the same time as other topical analgesics Stop use and consult a doctor if Condition worsens redness is present Irritation develops Symptoms persist for more than 7 days or clear up and occur again within a few days You experience signs of skin injury such as pain, swelling, or blistering where the product was applied. If pregnant of breastfeeding, ask a health professional before use Keep Out of Reach of Children. Do not use on infants. If swallowed, seek medical help or contact a Poison Control Centre right away.

Reported adverse events (FAERS/openFDA)#

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