Scott Clear Corn Removers

Manufacturer: Creative Foam Corporation
Effective date: 2025-12-05
Label type: HUMAN OTC DRUG LABEL
Version: 7
Source: full-release
Hydrated at: 2026-06-01 01:20:27

Label at a glance#

ProductScott Clear Corn Removers

Active ingredientSALICYLIC ACID

Label structure11 sections

Indications and uses

For removal of corns Relieves pain by removing corns

Dosage and administration

Wash affected area, dry thoroughly If necessary, cut medicated disk to fit corn Apply medicated disk with sitcky side adhereing to skin Cover medicated disk with enclosed cushion After 48 hours, remove disk Repeat procedure every 48 hours as needed for up to 14 days (until corn is removed) May soak corn in warm water for 5 minutes to a

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 40% w/w

Purpose

OTC - PURPOSE SECTION

Corn Removal

Uses

INDICATIONS & USAGE SECTION

For removal of corns
Relieves pain by removing corns

Warning

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 area that is infected or reddened

OTC - STOP USE SECTION

Stop use and ask a doctor if discomfort lasts

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 immediately.

Directions:

DOSAGE & ADMINISTRATION SECTION

Wash affected area, dry thoroughly
If necessary, cut medicated disk to fit corn
Apply medicated disk with sitcky side adhereing to skin
Cover medicated disk with enclosed cushion
After 48 hours, remove disk
Repeat procedure every 48 hours as needed for up to 14 days (until corn is removed)
May soak corn in warm water for 5 minutes to a

Other Information

OTHER SAFETY INFORMATION

Store between 15 ^o C and 30 ^o C (59 ^o F and 86 ^o F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Vinyl Acetate

Scott Clear Corn Removers

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Scott Clear Corn Removers

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
240559	salicylic acid 40 % Medicated Patch	PSN	7
240559	salicylic acid 0.4 MG/MG Medicated Patch	SCD	7
240559	salicylic acid 40 % Medicated Patch	SY	7

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0033116550008	GTIN-13: 0033116550008 EAN-13: 0033116550008 GTIN-12: 033116550008 UPC-A: 033116550008 GTIN storage (14 digits): 00033116550008	Scott Corn Removers.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
82660-006-05	Scott Clear Corn Removers	100 mg in 1 BOX	PLASTER	100		7

Products#

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

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

Scott Clear Corn Removers
40% w/w Salicylic Acid Corn Remover
POLYVINYL ALCOHOL, UNSPECIFIED
ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S)
SALICYLIC ACID

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
82660-006	82660-006-05

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
POLYVINYL ALCOHOL, UNSPECIFIED	532B59J990	IACT
ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S)	1PEZ3NLY6I	IACT
SALICYLIC ACID	O414PZ4LPZ	ACTIB

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
Scott Clear Corn Removers	40% W/W SALICYLIC ACID CORN REMOVER	Creative Foam Corporation	dd949b90-2f11-75eb-e053-2995a90af5a5	2025-12-05	Warnings	Exact identifier ndc (package): 82660-006-05 ndc (product): 82660-006 ndc11 (package): 82660000605 spl id: 4539780a-cdb1-bbdc-e063-6394a90a3169 spl set id: dd949b90-2f11-75eb-e053-2995a90af5a5

Reported adverse events (FAERS/openFDA)#

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