Premier Solutions Medicated Callus Removers

Manufacturer: Premier Brands of America Inc
Effective date: 2026-05-27
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 01:58:56

Label at a glance#

ProductMedicated Callus Removers

Active ingredientSALICYLIC ACID

Label structure9 sections

Indications and uses

for the removal of calluses relieves pain by removing calluses

Dosage and administration

wash affected area and dry thoroughly if necessary, cut medicated patch to fit callus carefully adhere medicated patch direclty over callus cover medicated patch with pad after 48 hours, remove medicated patch repeat this procedure every 48 hours as needed for up to 14 days (until callus is removed) may soak callus in warm water for 5 minutes to assist in removal

Contacts and useful links#

PhoneLabel contact1-866-964-0939

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 40%

Purpose

OTC - PURPOSE SECTION

Callus remover

Uses

INDICATIONS & USAGE SECTION

for the removal of calluses
relieves pain by removing calluses

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

if you are a diabetic
if you have poor blood circulation
on irritated skin or on any area that is infected or reddened

Stop use and ask a doctor if

OTC - ASK DOCTOR 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 affected area and dry thoroughly
if necessary, cut medicated patch to fit callus
carefully adhere medicated patch direclty over callus
cover medicated patch with pad
after 48 hours, remove medicated patch
repeat this procedure every 48 hours as needed for up to 14 days (until callus is removed)
may soak callus in warm water for 5 minutes to assist in removal

Other information

OTHER SAFETY INFORMATION

store between 15° to 30°C (59°F and 86°F)
avoid surrounding skin when applying medicated patch

Inactive ingredients

INACTIVE INGREDIENT SECTION

acrylic adhesive, acrylic polymer, polyethylene, polyvinyl alcohol

Questions?

OTC - QUESTIONS SECTION

call 1-866-964-0939

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

premier
solutions

Medicated
CALLUS
REMOVERS

SALICYLIC ACID 40% / CALLUS REMOVER

MAXIMUM STRENGTH
Effective callus removal treatment
Protects against pressure & friction

6 Pads

4 Medicated Patches

carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
240559	salicylic acid 40 % Medicated Patch	PSN	1
240559	salicylic acid 0.4 MG/MG Medicated Patch	SCD	1
240559	salicylic acid 40 % Medicated Patch	SY	1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
56104-913-01	Medicated Callus Removers	1 g in 1 PATCH	PATCH	1		1
56104-913-01	Medicated Callus Removers	4 in 1 BOX	PATCH	4		1

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Medicated Callus Removers
Salicylic Acid
HIGH DENSITY POLYETHYLENE
POLYVINYL ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
56104-913	56104-913-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
HIGH DENSITY POLYETHYLENE	UG00KM4WR7	IACT
SALICYLIC ACID	O414PZ4LPZ	ACTIB
POLYVINYL ALCOHOL	532B59J990	IACT

Source Document#

Source XML

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
Medicated Callus Removers	SALICYLIC ACID	Premier Brands of America Inc	52d0b36c-b65e-00cf-e063-6294a90ad089	2026-05-27	Warnings	Exact identifier ndc (package): 56104-913-01 ndc (product): 56104-913 ndc11 (package): 56104091301 spl id: 52d0b459-aa10-27a6-e063-6294a90ac58f spl set id: 52d0b36c-b65e-00cf-e063-6294a90ad089

Reported adverse events (FAERS/openFDA)#

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