FDA label 1b8bdd58-ee10-717b-e063-6294a90a4487

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
616f6295-4579-efa5-e053-2991aa0a7dad
SPL ID
1b8bdd58-ee10-717b-e063-6294a90a4487
Version
6
Effective date
2024-06-23
Source export date
2026-11-06
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/5731a8c92e1c0dd2a09d2f92b410e7a70ea29cbf6b8040a6a05e4be5b7c51f0d/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:40:21

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 salicylates Stop use and ask a doctor if - rash, itching, or excessive skin irritation develops - conditions worsen - symptoms persist for more than 5-6 days - symptoms clear up and occur again within a few days If pregnant or breast-feeding, ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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