FDA label 2a253f55-fd00-9b03-e063-6294a90ae571

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
290cac02-039a-bd07-e063-6294a90a886b
SPL ID
2a253f55-fd00-9b03-e063-6294a90ae571
Version
3
Effective date
2024-12-25
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:34:46

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

1. Do not use if you have skin conditions, eczema, or allergies. 2. If you experience swelling, pain, or red spots on the skin during use, stop using immediately and consult a physician. 3. Recommended use is up to 8 hours per day. 4. Store any unused patches in the resealable pouch to maintain effectiveness. 5. Keep out of reach of infants and children. 6. Do not use for purposes other than intended, and keep away from fire. 7. Avoid storing in temperatures above 30°C or in direct sunlight. Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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