FDA label e7c6be23-35f3-49cc-b68d-ca212c06ffd5

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
5f5387d9-c36b-49c6-a9c8-41f9b6fa804f
SPL ID
e7c6be23-35f3-49cc-b68d-ca212c06ffd5
Version
2
Effective date
2024-11-13
Source export date
2026-09-28
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:15:59

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 Do not use • more than 1 patch at a time • on wounds or damaged skin • with a heating pad • if you have ever had an allergic reaction to this product or any of its ingredients When using this product • use only as directed • avoid contact with the eyes, mucous membranes or rashes • do not bandage tightly Stop use and ask a doctor if • localized skin reactions occur, such as rash, itching, redness, irritation, pain, swelling and blistering • conditions worsen • symptoms persist for more than 7 days • symptoms clear up and occur again within a few days If pregnant or breast-feeding, ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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