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
2026-09-28
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 05:13:18

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.