FDA label 0aa3499b-1310-d2ca-e063-6294a90a7acd

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
ce48f4fe-912e-4bd2-e053-2995a90a6162
SPL ID
0aa3499b-1310-d2ca-e063-6294a90a7acd
Version
2
Effective date
2023-11-20
Source export date
2026-10-30
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-30/023bc8d8aae5addb7530087bbbdb169b3ccbf36764f15b8ca67db07e1e5aea8b/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run
20261102T182004Z
Imported at
2026-11-02 19:10:54

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 ■ irritated or damaged skin ■ sensitive skin ■ with a heating pad ■ if pregnant ■ with, or as the same time as, other external analgesic P.roducts ■ if allergic to aspirin or salicylates ■ 1f allergic to any ingredients of this product When using this product ■ avoid contact with the eyes ■ do not bandage tightly ■ do not apply to wounds or damaged skin ■ do not use more than 3 plasters a day ■ do not use 1 hour before or after bathing Stop use and ask a doctor if ■ condition worsens ■ symptoms persist for more than 7 days ■ symptoms clear up and occur again within a few days ■ excessive irritation of the skin develops ■ rashes, itching or redness are present ■ side effects occur. If pregnant. ask a health professional before use. Keep out of reach of children to avoid accidental poisoning In case of overdose, get medical help or contact a Poison Control Center right away. Do not use otherwise than as directed.

Reported adverse events (FAERS/openFDA)#

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