FDA label 95bef05e-3aec-4a27-ab4f-24b2567c8305

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
bb5aba25-6e5a-4c7e-a485-764e589b08b9
SPL ID
95bef05e-3aec-4a27-ab4f-24b2567c8305
Version
4
Effective date
2017-11-08
Source export date
2026-10-12
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/7928c8e8c6256620071a8b7e5b93eb8dfa543649c08d17a01ea02251012ba58c/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:26:20

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 • do not get into eyes or on mucous membranes • do not apply to wounds or to damaged or very sensitive skin • do not bandage tightly or cover with any type of wrap except clothing • do not use with a heating pad or apply external heat • do not use in combination with other external analgesic products Stop use and ask a doctor if • condition worsens • excessive redness, irritation, burning, or discomfort of the skin develops • pain persists for more than 7 days • symptoms clear up and occur again within a few days 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.