FDA label 1b8cb18a-59cd-2eee-e063-6294a90aefda

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
82ca29cf-5aa5-e8bf-e053-2a91aa0a8786
SPL ID
1b8cb18a-59cd-2eee-e063-6294a90aefda
Version
7
Effective date
2024-06-23
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 05:12:45

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 skin if you are allergic to any ingredients of this product with a heating pad with, or at the same time as, other external analgesic products When using this product do not use otherwise than directed avoid contact with eyes, mucous membranes or rashes do not bandage tightly Ask a doctor before use if you are prone to allergic reaction from aspirin or salicylate Stop use and ask a doctor if rash, itching, or excessive skin irritation develops conditions worsen symptoms persist for more than 7 days symptoms 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.