SALZIX WART REMOVER

Manufacturer
Toprail Chp Llc
Effective date
2025-03-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:02:06

Label at a glance#

ProductSALZIX WART REMOVER
Active ingredientSALICYLIC ACID
Label structure10 sections

Dosage and administration

• wash affected area, may soak wart in warm water for 5 minutes • dry area thoroughly • carefully apply one drop at a time with applicator to sufficiently cover each wart • let dry • repeat this procedure once or twice daily as needed (until wart is removed) for up to 12 weeks

Storage and handling

• store between 20°-25°C (68°-77°F) • close tightly to prevent solidification • wipe top of bottle clean after each use • discard when signs of wart no longer appear • avoid surrounding skin when applying product • do not allow to come into contact with fabrics, floors, countertops or other surfaces - will stain

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 17% w/w

Purpose

OTC - PURPOSE SECTION

Wart remover

Use

INDICATIONS & USAGE SECTION

• for the removal of common warts and plantar warts on the bottom of the foot. The common wart is easily recognized by the rough 'cauliflower-like' appearance of the surface. The plantar wart is recognized by its location only on the bottom of the foot, its tenderness, and the interruption of the footprint pattern.

Warnings

WARNINGS SECTION

For external use only.

Flammable • keep away from fire or flame

Do not use • if you are diabetic of if you have poor blood circulation
• on genital warts or warts on the face or mucous membrane
• on moles, birthmarks or warts with hair growing from them
• on irritated skin or on any area that is infected or reddened

When using this product • If product gets into the eye, flush with water for 15 minutes • avoid inhaling vapors • cap bottle tightly and store at room temperature away from heat

Stop use and ask a doctor if discomfort persists.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• wash affected area, may soak wart in warm water for 5 minutes • dry area thoroughly • carefully apply one drop at a time with applicator to sufficiently cover each wart • let dry • repeat this procedure once or twice daily as needed (until wart is removed) for up to 12 weeks

Other information

STORAGE AND HANDLING SECTION

• store between 20°-25°C (68°-77°F) • close tightly to prevent solidification • wipe top of bottle clean after each use • discard when signs of wart no longer appear • avoid surrounding skin when applying product • do not allow to come into contact with fabrics, floors, countertops or other surfaces - will stain

Inactive ingredients

INACTIVE INGREDIENT SECTION

camphor, castor oil, ethanol, ethyl ether, nitrocellulose

Questions?

OTC - QUESTIONS SECTION

Call 1-866-964-0939

SPL UNCLASSIFIED SECTION

• Removes Common & Plantar Warts
• Convenient Brush Applicator
• Safe & Effective
• Maximum Strength
• Fast Acting Liquid

IMPORTANT: CLOSE CAP TIGHTLY AFTER USE

DO NOT USE IF NECKBAND IS BROKEN

DISTRIBUTED BY:
TOPRAIL PHARMACEUTICALS
NORTHBROOK, IL
www.TOPRAILPHARMACEUTICALS.com

​MADE IN USA FROM GLOBALLY SOURCED MATERIALS

Keep packaging for complete drug facts information.

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SALZIX WART REMOVERSALZIX WART REMOVER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72847-333-29SALZIX WART REMOVER1 in 1 BOXLIQUID11
72847-333-29SALZIX WART REMOVER9 mL in 1 BOTTLE, WITH APPLICATORLIQUID91

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72847-33372847-333-29

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SALZIX WART REMOVERSALICYLIC ACIDToprail Chp Llc69864363-ecd7-4b08-ba9e-ecd1a3e95f372025-03-20WarningsExact identifier
ndc (package): 72847-333-29
ndc (product): 72847-333
ndc11 (package): 72847033329
spl id: b71df063-c5d7-4a4f-a638-f004158631e4
spl set id: 69864363-ecd7-4b08-ba9e-ecd1a3e95f37

Reported adverse events (FAERS/openFDA)#

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