Liquid Corn and Callus Remover

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)

Brand name
Liquid Corn and Callus Remover
Generic name
SALICYLIC ACID
Manufacturer
Meijer Distribution Inc
Product type
HUMAN OTC DRUG
SPL set ID
039c3dbe-97ba-805c-e063-6394a90a91e8
SPL ID
40abbec6-fc17-9c88-e063-6394a90a8d19
Version
5
Effective date
2025-10-08
Source export date
2026-10-12
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/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:44:58
Harmonized routes table
Harmonized routes
TOPICAL

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

Warnings For external use only. Flammable keep away from fire or flame Do not use on irritated skin on any area that is infected or reddened if you are a diabetic, or if you have poor blood circulation When using this product if product gets into the eye, flush with water for 15 minutes avoid inhaling vapors cap bottle tightly and store at room temperature away from heat Stop and ask a doctor if discomfort persists. 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.