Liquid Callus Remover

Manufacturer: Premier Brands of America Inc.
Effective date: 2025-10-08
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-06-01 01:38:15

Label at a glance#

ProductLiquid Callus Remover

Active ingredientSALICYLIC ACID

Label structure8 sections

Indications and uses

for the removal of corns and calluses relieves pain by removing corns and calluses

Dosage and administration

wash the affected area and dry thoroughly apply one drop at a time with applicator to sufficiently cover each corn/callus let dry repeat this procedure once or twice daily as needed for up to 14 days (until corn/callus is removed) may soak corn/callus in warm water for 5 minutes to assist in removal

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 17% w/w

Purpose

OTC - PURPOSE SECTION

Corn and callus remover

Uses

INDICATIONS & USAGE SECTION

for the removal of corns and calluses
relieves pain by removing corns and calluses

Warnings

WARNINGS SECTION

For external use only.

Flammable

SAFE HANDLING WARNING SECTION

keep away from fire or flame

Do not use

OTC - DO NOT USE SECTION

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

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

discomfort persists

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

wash the affected area and dry thoroughly
apply one drop at a time with applicator to sufficiently cover each corn/callus
let dry
repeat this procedure once or twice daily as needed for up to 14 days (until corn/callus is removed)
may soak corn/callus in warm water for 5 minutes to assist in removal

Other information

OTHER SAFETY INFORMATION

store between 20° to 25°C (68° to 77°F)
avoid surrounding skin when applying product
close tightly to prevent solidification
wipe top of bottle clean after each use
do not allow to come into contact with fabrics, floors, countertops or other surfaces -- will stain

Inactive ingredients

INACTIVE INGREDIENT SECTION

camphor, castor oil, ethanol, ethyl ether, nitrocellulose

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

EndZone

LIQUID

CALLUS

REMOVER

SALICYLIC ACID 17% / CORN & CALLUS REMOVER

Safely removes corns & calluses

0.33 FL OZ (9.8 mL) Image 1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
312881	salicylic acid 17 % Topical Solution	PSN	4
312881	salicylic acid 170 MG/ML Topical Solution	SCD	4
312881	salicylic acid 17 % Topical Solution	SY	4

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277	Product name	1	20190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
56104-501-00	Liquid Callus Remover	1 in 1 CARTON	LIQUID	1		4
56104-501-00	Liquid Callus Remover	9.8 mL in 1 BOTTLE, WITH APPLICATOR	LIQUID	9.8		4

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

Liquid Callus Remover
Salicylic Acid
CASTOR OIL
PYROXYLIN
CAMPHOR (NATURAL)

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
56104-501	56104-501-00

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CASTOR OIL	D5340Y2I9G	IACT
SALICYLIC ACID	O414PZ4LPZ	ACTIB
PYROXYLIN	KYR8BR2X6O	IACT
CAMPHOR (NATURAL)	N20HL7Q941	IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
3	2024-10-14	full-release	2026-06-01 00:25:02

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Liquid Callus Remover	SALICYLIC ACID	Premier Brands of America Inc.	051c7917-76ea-c7f8-e063-6394a90a9e36	2025-10-08	Warnings	Exact identifier ndc (package): 56104-501-00 ndc (product): 56104-501 ndc11 (package): 56104050100 spl id: 40aba81a-36f9-82cc-e063-6394a90a3b06 spl set id: 051c7917-76ea-c7f8-e063-6394a90a9e36

Reported adverse events (FAERS/openFDA)#

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