FDA label 4a8a9ec2-6fc1-4881-8a5b-a4f229933cfc

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
8bd794d6-399a-4b11-8f65-9b620099f913
SPL ID
4a8a9ec2-6fc1-4881-8a5b-a4f229933cfc
Version
1
Effective date
2014-10-16
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 05:29:33

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

Warning Callus Removal Foot Pack is not suitable for patients with Glucose -6-Phosphate Dehydrogenase deficiency (G6PD), pregnant woman, Reye's syndrome, patients intolerant to salicylate or diabetic patients. Avoid prolonged and excessive use on large area of body or on broken or inflamed skin. Avoid contact with eyes, mouth or other mucous membrane. If there is any redness, swelling, itchiness, inflammation or other symptoms of the skin, please stop using it. keep out of direct sun light and high temperature. Use immediately after opening .This is the disposable merchandise. Dispose the foot packs after use.

Reported adverse events (FAERS/openFDA)#

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