Scholls Wellness Company LLC

Manufacturer
Scapa Tapes North America LLC
Effective date
2022-01-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:11:51

Label at a glance#

ProductScholls Wellness Company LLC Liquid Corn and Callus Remover
Active ingredientSALICYLIC ACID
Label structure14 sections

Indications and uses

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

Dosage and administration

Directions​ wash affected area and dry thoroughly apply one drop at a time with applicator to sufficiently cover each corn/callus let dry repeat 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 protective pads may be used to cushion corn/callus during treatment

Label contents#

Full prescribing information#

Drug Facts

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient Purpose

Salicylic Acid 17%w/w.......................Corn and callus remover

Purpose

OTC - PURPOSE SECTION

Corn and callus remover

Uses

INDICATIONS & USAGE SECTION

Uses

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

Warnings

WARNINGS SECTION

Warnings

For external use only

Flammable: Keep away from fire or flames.

Do not use

OTC - DO NOT USE SECTION

Do not use

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

When using this product

OTC - WHEN USING SECTION

When using this product

if product gets in eyes, flush with water for 15 minutes

do not inhale vapors

cap bottle tightly and store at room temperature away from heat

Stop use and ask a doctor

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if discomfort lasts

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed,

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

Directions

DOSAGE & ADMINISTRATION SECTION

Directions​

wash affected area and dry thoroughly

apply one drop at a time with applicator to sufficiently cover each corn/callus

let dry

repeat 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

protective pads may be used to cushion corn/callus during treatment

Other Information

OTHER SAFETY INFORMATION

Other information​

store between 20ºC to 25ºC (68º to 77ºF)

keep tightly closed

retain card for full labeling

INACTIVE INGREDIENT SECTION

Inactive ingredients​ castor oil, ethyl lactate, flexible collodion, polybutene. (Contains alcohol 18% v/v and ether 53% v/v from flexible collodion)

OTC - QUESTIONS SECTION

Questions? 1-866-360-3226

Liquid Corn & Callus Remover Salicylic Acid

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Corn & Callus Remover Salicylic AcidCorn & Callus Remover Salicylic Acid

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66843-04666843-046-41

Ingredients#

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

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

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d672cdb2-6cb3-53ee-e053-2995a90a41a7d672d35a-6a06-362f-e053-2995a90a9ce12022-01-25WarningsExact identifier
spl id: d672cdb2-6cb3-53ee-e053-2995a90a41a7
spl set id: d672d35a-6a06-362f-e053-2995a90a9ce1

Reported adverse events (FAERS/openFDA)#

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