FDA.reportPublic FDA data

FDA label dd2063a6-b3e3-4583-b960-daa2bf27d325

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
149b1382-5b3a-4390-9ce6-74cdbf3d3984
SPL ID
dd2063a6-b3e3-4583-b960-daa2bf27d325
Version
2
Effective date
2025-12-02
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 07:25:12

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 2 matching rows.

warnings

Warnings For external use only When using this product: ■ Use only as directed ■ Avoid contact with eyes ,mucous membranes or rashes ■ Do not apply to broken, wounded or damaged skin ■ Do not bandage or cover with any type of wrap except clothing ■ Do not use with a heating pad or apply external heat ■ Discontinue use at least 1 hour before a bath or shower and do not use immediately after a bath or shower

warnings and cautions

Warning and Precautions Do not apply on Ulcerative or suppurative skin area Not be used by during pregnancy This product may cause allergic reaction in some individuals.

Reported adverse events (FAERS/openFDA)#

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