FDA label 2a83cb8f-eea0-2e45-e063-6394a90a7365

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
86acfc88-2322-b097-e053-2a91aa0a032f
SPL ID
2a83cb8f-eea0-2e45-e063-6394a90a7365
Version
5
Effective date
2024-12-30
Source export date
2026-09-28
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:14:24

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 Flammable Keep away from excessive heat or open flame Do Not Use On damaged or irritated skin With a bandage or heating pad If you are allergic to any ingredients in this product Other than as directed When Using This Product Avoid contact with the eyes Stop Use and Ask a Doctor If Condition worsens Excessive skin irritation develops Symptoms persist for more than 7 days, or symptoms clear up and occur again within 3 days If You Are Pregnant or Breast Feeding Ask a health professional before use Keep Out of Reach of Children If ingested, seek medical help or contact a Poison Control Center immediately

Reported adverse events (FAERS/openFDA)#

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