FDA label 315fd1be-ae83-460e-96ac-e8117ded1dd7

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
09d6b5a1-9223-4b60-b92d-7883a434a13e
SPL ID
315fd1be-ae83-460e-96ac-e8117ded1dd7
Version
1
Effective date
2017-02-21
Source export date
2026-10-12
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:04:34

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 otherwise than as directed if you are allergic to any ingredient in this product on a child under 12 years of age with arthritis-like conditions with a heating pad When using this product avoid contact with eyes, wounds, mucous membranes, broken or irritated skin do not share this product with anyone do not bandage tightly Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days skin redness or excessive irritation of the skin develops If pregnant or breast-feeding, ask a health professional before use. Keep out of the reach of children. If swallowed, get mediacal help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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