FDA label 6cb7a46a-84aa-43fb-8da2-c33ddf573f0b

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
2e153c5c-bb12-42db-bd70-c9b68a6ffa0f
SPL ID
6cb7a46a-84aa-43fb-8da2-c33ddf573f0b
Version
1
Effective date
2014-04-14
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 07:41:59

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. When using this product Avoid contact with eyes or mucous membranes. Do not apply to open wounds or damaged skin. Do not bandage or use heating pad. Stop use and ask a doctor Condition worsens Severe skin irritation occurs Pain persistes for more than seven days. Pain clears up and then recurs a few days later If pregnant or breast-feeding ask a healthcare professional before use. Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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