FDA label 824b603a-7647-9006-e053-2a91aa0a172e

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
81ac3ab3-ff11-5b52-e053-2a91aa0a51b9
SPL ID
824b603a-7647-9006-e053-2a91aa0a172e
Version
2
Effective date
2019-02-19
Source export date
2026-10-12
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 03:00:11

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 - It is normal that the product heats the attached area, but if a rash appears on the skin, stop using the product immediately and go to see a doctor. - Those who have sensitive skin or dermatitis should avoid long-hour usage(over 5 hours). - Be careful using the product before or after sauna and hot massage when your skin may be more sensitive than the usual. - If you feel itchy, remove the patch immediately and wash off the area with cold water. - Do NOT use the product during pregnancy. - Do NOT use the product to infants/children under 30 months. - This product is NOT a medicine, but one of the manufactured goods.

Reported adverse events (FAERS/openFDA)#

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