FDA label 26fa692d-8bff-4c2c-a77f-8a4312da2678

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
e1aee637-2cab-489e-b359-908d744f85ce
SPL ID
26fa692d-8bff-4c2c-a77f-8a4312da2678
Version
1
Effective date
2023-12-12
Source export date
2026-10-12
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:41:22

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, broken, or irritated skin • with a heating pad • at the same time with other topical analgesics Ask a doctor before use if you have • redness over affected area When using this product • avoid contact with the eyes, mucous membranes, and rashes • do not bandage tightly Stop use and ask a doctor if • condition worsens or symptoms persist for more than 7 days or clear up and occur again within a few days • abnormal skin irritation occurs after usage If pregnancy or breastfeeding , ask a health 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.