FDA label 460c376c-3027-2460-e063-6394a90a0089

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
460c376c-3026-2460-e063-6394a90a0089
SPL ID
460c376c-3027-2460-e063-6394a90a0089
Version
1
Effective date
2025-12-16
Source export date
2026-10-12
Source partition
14
Source file
https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/acb9b4700b9af1bdda1c389c7b35bfe38fd6d1a62aa48d17832812be4029b84f/drug-label-0014-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 03:13:19

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.For external use only. 2.Allergy alert: lf prone to allergic reaction from aspirin or salicylates, consult a doctor before use3.Do not use: On wounds or damaged skin. With a heating pad. lf you are allergic to anyingredients of this product. 4.When using this product: Use only as directed. Avoid contact with the eyes. mucousmembranes or rashes. Do not bandage tightly 5.Stop using it and ask a doctor if: Skin reactions such as redness, itching, rash, excessiveirritation, burning sensation,swelling or blistering occur. Conditions worsen.Symptomspersist for more than 7 days. Symptoms clear up and occur again within a few days6.Pregnancy/breast-feeding warning: lf pregnant or breast-feeding, ask a healthprofessional before use.

Reported adverse events (FAERS/openFDA)#

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