Salicylic acid

Manufacturer: Target Corporation
Effective date: 2024-12-18
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: legacy-cache
Hydrated at: 2026-08-01 20:45:19

Label at a glance#

ProductSalicylic acid

Active ingredientSALICYLIC ACID

Label structure9 sections

Dosage and administration

wash affected area and dry area thoroughly if necessary, cut medicated patch to fit callus apply adhesive side down of medicated patch onto callus cover medicated patch with pad after 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

Callus remover

Use

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, on any area that is infected or reddened

Stop use and ask a doctor

OTC - ASK DOCTOR SECTION

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 callus
apply adhesive side down of medicated patch onto callus
cover medicated patch with pad
after 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

callus removers

salicylic acid 40%

effective callus removal treatment

extra thick pads cushion & help

protect against pressure & friction

4 PADS/ 4 MEDICATED PATCHES carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
11673-631-04	2024-12-18	C162847	48780-1	f386c64a-248e-0266-e053-dadaa90a7c1a	Target Extra Thick Callus Removers
11673-631-04	2023-01-30	C162847	48780-1	f386c64a-248e-0266-e053-dadaa90a7c1a	Target Extra Thick Callus Removers

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
11673-631	SALICYLIC ACID (MEDICATED CALLUS REMOVERS EXTRA THICK) PATCH [TARGET CORPORATION]	5	Legacy NDC	20241220_6e2509ab-ec8f-4e2d-b1b5-0b547a11d319.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 Callus Removers Extra Thick
POLYVINYL ALCOHOL
VINYL ACETATE
HIGH DENSITY POLYETHYLENE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
11673-631	11673-631-04

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
37c727d4-08ee-af8d-e063-6294a90a78e1			6e2509ab-ec8f-4e2d-b1b5-0b547a11d319	2025-06-17	Warnings	Exact identifier spl set id: 6e2509ab-ec8f-4e2d-b1b5-0b547a11d319

Reported adverse events (FAERS/openFDA)#

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