FDA label 91725e40-3f33-43ad-80a5-5accb0b34d2b

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
a4fc913f-18ce-4d8d-9a59-be9522cdb1d8
SPL ID
91725e40-3f33-43ad-80a5-5accb0b34d2b
Version
2
Effective date
2018-10-26
Source export date
2026-10-12
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 03:04:04

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 the face ● on wounds or damaged skin or irritated skin ● with heating pad or device ● with, or at the same time as, other external analgesic products ● right before or after heart surgery Ask a doctor before use if ● you are prone to allergic reaction ● you are allergic to topical products When using this product ● avoid contact with eyes, mucous membranes or rashes ● do not bandage tightly ● do not use otherwise than directed Stop use and ask a doctor if ● Condition worsens ● if symptoms persist for more than 7 days or clear up occur again within a few days ● rash, itching or excessive skin irritation develops If pregnant or breast-feeding, ask a health professional before use while breast-feeding and during the first 6 months of pregnancy. Do not use during the last 3 months of pregnancy because it may cause problems in the unborn child or complications during delivery. Or ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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