FDA label 50bb5c9f-072a-478f-9c42-bbd04e20d49b

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
5e081d6c-0619-4d6c-be50-588c488404eb
SPL ID
50bb5c9f-072a-478f-9c42-bbd04e20d49b
Version
1
Effective date
2017-03-17
Source export date
2026-10-12
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/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:05:16

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 on open sores. Ask a doctor before use if you have diabetes poor blood circulation gout When using this product use with a retainer ring avoid contact with eyes. If prodcut gets into the eye, flush with water for 15 minutes and get medical help reight away. Stop use and ask a doctor if redness or swelling of your toe increases discharge is present around the nail symptoms last more than 7 days or clear up and occur again within a few days Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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