Salicylic Acid

Manufacturer: Target Corporation
Effective date: 2024-12-11
Label type: HUMAN OTC DRUG LABEL
Version: 8
Source: legacy-cache
Hydrated at: 2026-08-01 20:46:56

Label at a glance#

ProductSalicylic Acid

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 area thoroughly if necessary, cut medicated patch to fit corn apply adhesive side down of medicated patch onto corn cover medicated patch with padafter 48 hours, remove medicated patch 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

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

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

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

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if 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 area thoroughly
if necessary, cut medicated patch to fit corn
apply adhesive side down of medicated patch onto corn
cover medicated patch with padafter 48 hours, remove medicated patch
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

OTHER SAFETY INFORMATION

store between 15°C to 30°C (59°F to 86°F)

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

medicated

corn removers

salicylic acid 40%

cushioned pads help protect against pressure and friction

effective corn removal treatment

9 MEDICATED PATCHES / 9 PADS

Corn Removers

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
11673-630-09	2023-01-31	C162847	48780-1	f386c649-d9d3-0266-e053-dadaa90a7c1a	Target Medicated Corn Removers

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
11673-630	SALICYLIC ACID (MEDICATED CORN REMOVERS) PATCH [TARGET CORPORATION]	8	Legacy NDC	20241213_ca6aa432-59f1-4006-9152-8e71d0b68708.zip

Products#

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

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

Salicylic Acid
Medicated Corn Removers
POLYVINYL ALCOHOL
VINYL ACETATE
HIGH DENSITY POLYETHYLENE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
11673-630	11673-630-09

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
POLYVINYL ALCOHOL	532B59J990	IACT
VINYL ACETATE	L9MK238N77	IACT
HIGH DENSITY POLYETHYLENE	UG00KM4WR7	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
37c7e5fc-e094-4bb7-e063-6294a90a31a1			ca6aa432-59f1-4006-9152-8e71d0b68708	2025-06-17	Warnings	Exact identifier spl set id: ca6aa432-59f1-4006-9152-8e71d0b68708

Reported adverse events (FAERS/openFDA)#

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