FDA label eee53321-ca57-416f-8c1e-36f205a387a7

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
883d2910-084b-4a80-b30e-e7bdff8087ce
SPL ID
eee53321-ca57-416f-8c1e-36f205a387a7
Version
1
Effective date
2015-12-17
Source export date
2026-10-12
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:33:55

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: Take out a little essence after cutting a tiny hole of the callus removal foot pack and smear on an area of foot for testing its reaction before using the mask. Wait around 60 minutes, then wash away lotion and dry your foot. If there is any redness, swelling, itching, inflammation or other uncomfortable symptoms, please refer to your doctor before using it.

Reported adverse events (FAERS/openFDA)#

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