FDA label 64dd6d69-41a1-176c-e053-2a91aa0a4dec

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
64dd6d69-41a0-176c-e053-2a91aa0a4dec
SPL ID
64dd6d69-41a1-176c-e053-2a91aa0a4dec
Version
3
Effective date
2018-02-10
Source export date
2026-09-28
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:30:44

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 When using this product Use only as directed. - Do not bandage tightly or use with heating pad - Avoid contact with eyes and mucus membranes - Do not appy wounds or broken skin - Do not apply to large areas of the body - In case of deep or puncture wounds, animal bites or serious burns, consult a doctor Stop use and ask a doctor if - condition worsen - irritation develops - symptoms persist for more than 7 days or recurs within 1 day of discontinuation - do not use for more than 7 days If pregnant or breast-feeding, ask a health professional before use Keep out of reach of children. If swallowd, contact a Poison Control Center or get medical help immediately

Reported adverse events (FAERS/openFDA)#

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