FDA label ce7db22a-c116-4003-b991-63bd1f4689b9

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
d7b72e52-06a3-4e1e-a00a-533005ee981a
SPL ID
ce7db22a-c116-4003-b991-63bd1f4689b9
Version
1
Effective date
2011-09-16
Source export date
2026-10-22
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/2026-10-22/0bafccaf0213baa649cda9c1c2365d28432e10cf46f4167b2ea41290b5cac2b8/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
5de9d3c3492926d1703b492ae4d29b036ac5be73edfcb92a6cd5eb95a2acef9c
Import run
20261023T001338Z
Imported at
2026-10-23 00:58:14

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 WITH A HEATING PAD DO NOT BANDAGE TIGHTLY DO NOT SWALLOW If swallowed, induce vomiting and call a physician. Keep away from eyes, mucous membranes, broken or irritated skin. If redness or irritation develops, pain lasts more than 10 days or with arthritis-like conditions in children under 12, do not use and call a physician. KEEP AWAY FROM CHILDREN TO AVOID ACCIDENTAL POISONING. Enter section text here

Reported adverse events (FAERS/openFDA)#

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