Salicylic Acid Corn Remover

Manufacturer: ASO Pharmaceutical Co. Ltd.
Effective date: 2022-05-06
Label type: HUMAN OTC DRUG LABEL
Version: 6
Source: legacy-cache
Hydrated at: 2026-08-01 21:56:19

Label at a glance#

ProductSalicylic Acid Corn Remover

Active ingredientSALICYLIC ACID

Label structure9 sections

Indications and uses

for the removal of corns. relieves pain by removing corns

Dosage and administration

Wash affected area and dry thoroughly Remove medicated pad from backing paper by pulling from center of pad Apply After 48 hours, remove medicated pad 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 assist in removal

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 40%

Purpose

OTC - PURPOSE SECTION

Corn remover

Uses

INDICATIONS & USAGE SECTION

for the removal of corns.
relieves pain by removing corns

Warnings

WARNINGS SECTION

For External Use Only

Do not use

OTC - DO NOT USE SECTION

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

discomfort lasts

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Wash affected area and dry thoroughly
Remove medicated pad from backing paper by pulling from center of pad
Apply
After 48 hours, remove medicated pad
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 assist in removal

Other information

SPL UNCLASSIFIED SECTION

store at room temperature
avoid excessive heat 99ºF (37ºC)

Inactive ingredients

INACTIVE INGREDIENT SECTION

lanolin, polybutene, rosin ester, rubber

SPL UNCLASSIFIED SECTION

Distributed by:

ASO LLC
Sarasota, FL 34240

Made in Japan

*This product is not manufactured or distributed by he Bayer Corporation, owners of the registered trademark Dr. Scholl’s®.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ONE STEP

CORN REMOVER

MAXIMUM STRENGTH

SALICYLIC ACID 40%

Cushions & helps relieve pain
Convenient 1-step bandage
Waterproof

Front Panel Corn Remover

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
SALICYLIC ACID	ACTIVE INGREDIENT	O414PZ4LPZ	4
SALICYLIC ACID	ACTIVE MOIETY	O414PZ4LPZ	4
LANOLIN	INACTIVE INGREDIENT	7EV65EAW6H	4
NATURAL LATEX RUBBER	INACTIVE INGREDIENT	2LQ0UUW8IN	4

Products#

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

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

Salicylic Acid Corn Remover
Salicylic Acid
LANOLIN
NATURAL LATEX RUBBER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
51511-514	51511-514-01, 51511-514-24, 51511-514-18, 51511-514-08

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
LANOLIN	7EV65EAW6H	IACT
NATURAL LATEX RUBBER	2LQ0UUW8IN	IACT
SALICYLIC ACID	O414PZ4LPZ	ACTIB

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 9 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
LANOLIN	LANOLIN	7EV65EAW6H	OINTMENT / TOPICAL	10 %w/w		Exact identifier — unii candidate 9 equally ranked IID candidates
LANOLIN	LANOLIN	7EV65EAW6H	CREAM / TOPICAL		10 mg	Exact identifier — unii candidate 9 equally ranked IID candidates
LANOLIN	LANOLIN	7EV65EAW6H	SPRAY / NASAL	NA		Exact identifier — unii candidate 9 equally ranked IID candidates
LANOLIN	LANOLIN	7EV65EAW6H	LOTION / TOPICAL	1.5 %w/w		Exact identifier — unii candidate 9 equally ranked IID candidates
LANOLIN	LANOLIN	7EV65EAW6H	OINTMENT / OPHTHALMIC	3 %w/w		Exact identifier — unii candidate 9 equally ranked IID candidates
LANOLIN	LANOLIN	7EV65EAW6H	SHAMPOO / TOPICAL	2 %w/w		Exact identifier — unii candidate 9 equally ranked IID candidates
LANOLIN	LANOLIN	7EV65EAW6H	CREAM / VAGINAL	2 %w/w		Exact identifier — unii candidate 9 equally ranked IID candidates
LANOLIN	LANOLIN	7EV65EAW6H	EMULSION / TOPICAL	0.25 %w/w		Exact identifier — unii candidate 9 equally ranked IID candidates
LANOLIN	LANOLIN	7EV65EAW6H	OINTMENT / RECTAL		105 mg	Exact identifier — unii candidate 9 equally ranked IID candidates

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
e4df1cb1-c01a-286b-e053-2a95a90a97b6			66063960-643d-4351-a134-37a0eb4de6ed	2022-07-28	Warnings	Exact identifier spl set id: 66063960-643d-4351-a134-37a0eb4de6ed

Reported adverse events (FAERS/openFDA)#

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