Salicylic acid

Manufacturer: Rite Aid Corporation
Effective date: 2025-06-21
Label type: HUMAN OTC DRUG LABEL
Version: 7
Source: full-release
Hydrated at: 2026-06-01 01:03:33

Label at a glance#

ProductSalicylic acid

Active ingredientSALICYLIC ACID

Label structure9 sections

Dosage and administration

after washing affected area, soak wart for 5 minutes in comfortably warm water dry area thoroughly if necessary cut medicated patch to fit wart apply adhesive side down of patch onto wart cover patch with pad to conceal area repeat this procedure every 48 hours as needed (until wart is removed) for up to 12 weeks

Contacts and useful links#

PhoneLabel contact1-866-964-0939

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 40%w/w

Purpose

OTC - PURPOSE SECTION

Wart removal

Use

INDICATIONS & USAGE SECTION

For the removal of common warts. The common wart has a rough 'cauliflower-like' appearance..

Warnings

WARNINGS SECTION

For external use only.

Do not use this product if

OTC - DO NOT USE SECTION

you are a diabetic or have poor blood circulation, except under the advice and supervision of a doctor or podiatrist

Do not use on

OTC - DO NOT USE SECTION

irritated, infected or reddened skin
moles, birthmarks and warts with hair growing from them on
genital warts and warts on the face
mucous membranes

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.

If discomfort persists

OTC - ASK DOCTOR SECTION

see your doctor or podiatrist.

Directions

DOSAGE & ADMINISTRATION SECTION

after washing affected area, soak wart for 5 minutes in comfortably warm water
dry area thoroughly
if necessary cut medicated patch to fit wart
apply adhesive side down of patch onto wart
cover patch with pad to conceal area
repeat this procedure every 48 hours as needed (until wart is removed) for up to 12 weeks

Other information

OTHER SAFETY INFORMATION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

acrylic adhesive, polyethylene foam

Questions?

OTC - QUESTIONS SECTION

Call 1-866-964-0939

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Rite Aid

PHARMACY

wart

remover kit

salicylic acid

relieves painful warts

18 medicated patches

20 concealing pads

Rite Aid_Wart Remover Kit_WRKBRA-3.jpg

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277	Product name	1	20190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
11822-0134-1	Salicylic acid	18 in 1 BOX	PLASTER	18		7

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

Salicylic acid
Wart Remover
HIGH DENSITY POLYETHYLENE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
11822-0134	11822-0134-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
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
Salicylic acid	WART REMOVER	Rite Aid Corporation	01bb867a-be7c-416b-bb00-15894d06a029	2025-06-21	Warnings	Exact identifier ndc (package): 11822-0134-1 ndc (product): 11822-0134 ndc11 (package): 11822013401 spl id: 3810614c-25d4-d713-e063-6394a90a9890 spl set id: 01bb867a-be7c-416b-bb00-15894d06a029

Reported adverse events (FAERS/openFDA)#

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