FDA label c816905d-8e8c-4a89-9ccd-42e962ad29f4

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
aeaa8c1b-c443-427b-aea0-de440d9145a8
SPL ID
c816905d-8e8c-4a89-9ccd-42e962ad29f4
Version
2
Effective date
2017-11-22
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:41:22

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.