FDA label c836cc9a-9803-2b1f-e053-2995a90ae3a6

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
83e784ad-7858-4e08-b590-186b718d41cf
SPL ID
c836cc9a-9803-2b1f-e053-2995a90ae3a6
Version
3
Effective date
2021-07-28
Source export date
2026-09-28
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/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:13:57

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 • with other topical pain relievers •with heating pads or heating devices. When using this product do not use in or near eyes do not apply to wounds or damaged skin do not bandage tightly When using this product do not use in or near eyes do not apply to wounds or damaged skin do not bandage tightly Stop use and ask doctor if Conditions worsens symptoms last more than 7 days or clear up and occur again within a few days redness or irritation develop If pregnant or breast-feeding , ask a heath professional before use

Reported adverse events (FAERS/openFDA)#

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