FDA label b10e06e9-259c-4e88-9837-b0879799d424

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
0d8f2d13-3ce5-4ac7-afaf-c57f38ba4b62
SPL ID
b10e06e9-259c-4e88-9837-b0879799d424
Version
1
Effective date
2011-09-16
Source export date
2026-10-12
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:48:47

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.