FDA.reportPublic FDA data

FDA label dd7bc8f2-f847-4f65-9d38-95ac570b4f0b

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
e1d40780-4873-4e5b-a82b-a014a86c70a9
SPL ID
dd7bc8f2-f847-4f65-9d38-95ac570b4f0b
Version
2
Effective date
2016-11-04
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 bandage tightly • do not get into eyes or on mucous membranes • do not apply to wounds or damaged skin • 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 irritation, burning or discomfort of the skin develops • symptoms persist for more than 7 days or clear up and occur again within a few days

Reported adverse events (FAERS/openFDA)#

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