FDA label 4f82993c-ebc5-5787-e063-6294a90a12d6

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
4f82993c-ebc4-5787-e063-6294a90a12d6
SPL ID
4f82993c-ebc5-5787-e063-6294a90a12d6
Version
1
Effective date
2026-04-20
Source export date
2026-11-06
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/824fe785252d7061429a95ddb6de517ee399ef628d34e8fdcc3591ded286ae33/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:26:59

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

For external use only Do not use in large quantities on wounds, damaged, broken, or irritated skin for more than one week without consulting a doctor When using this product use only as directed. Read and follow all directions and warnings on this label avoid contact with the eyes and mucous membranes do not bandage tightly or apply local heat such as a heating pad or a medicated patch do not use with other topical analgesics ​Stop use and ask a doctor if rash or irritation develops symptoms worsen or persist for more than 7 days or clear up and occur again within a few days

Reported adverse events (FAERS/openFDA)#

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