FDA label 0bc4e3b7-24a6-435a-e054-00144ff88e88

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
07b43c31-a4d2-5c29-e054-00144ff88e88
SPL ID
0bc4e3b7-24a6-435a-e054-00144ff88e88
Version
8
Effective date
2014-11-01
Source export date
2026-11-06
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/2026-11-06/d05434af5edc4383b7c7894a8f2d94df21171d17714450933cecdfc35cedfa3d/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 06:43:48

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 Keep out reach of children If swallowed, get medical help or contact poison control center immediately. Do not use ■ on wounds or damaged skin. ■ with a heating pad ■ with, or at the same time as, other external analgesic products. ■ if you are allergic to any ingredients of this product. When using this product: ■ do not use otherwise than as directed. ■ avoid contact with eyes, mucous membranes or rashes. Stop use and consult a doctor for: ■ rash, itching or excessive skin irritation develops. ■ conditions worsen. ■ symptoms persist for more than7 days. ■ symptoms clear up and occur again within a few days. If swallowed, get medical help or contact poison control center immediately.

Reported adverse events (FAERS/openFDA)#

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