FDA.reportPublic FDA data

PediQuick OneStep Wart Removers

Manufacturer
PEDIFIX, INC, | PEDIFIX, INC. | AKRON COATING AND ADHESIVES
Effective date
2019-03-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:24:52

Label at a glance#

ProductPediQuick OneStep Wart Removers
Active ingredientSALICYLIC ACID
Label structure13 sections

Indications and uses

For the removal of common warts. The common wart is easily recognized by the rough ‘cauliflower-like’ appearance on the surface

Dosage and administration

wash affected area may soak in warm water for 5 minutes dry area thoroughly remove bandage from backing apply medicated strip, positioning medicated area directly over wart repeat procedure every 48 hours as needed (until wart is removed) fo up to 12 weeks

Storage and handling

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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 40%

Purpose

OTC - PURPOSE SECTION

Wart remover

Uses

INDICATIONS & USAGE SECTION

For the removal of common warts. The common wart is easily recognized by the rough ‘cauliflower-like’ appearance on the surface

Warnings

WARNINGS SECTION

For external use only

Do Not Use this product

OTC - DO NOT USE SECTION

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

If discomfort persists,

OTC - ASK DOCTOR SECTION

see your doctor or podiatrist.

Do nou use on

OTC - DO NOT USE SECTION

  • moles
  • birthmarks
  • warts with hair growing from them
  • genital warts
  • or warts on the face or mucus 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 immediately

Directions

INSTRUCTIONS FOR USE SECTION

  • wash affected area
  • may soak in warm water for 5 minutes
  • dry area thoroughly
  • remove bandage from backing
  • apply medicated strip, positioning medicated area directly over wart
  • repeat procedure every 48 hours as needed (until wart is removed) fo up to 12 weeks

Other Information

STORAGE AND HANDLING SECTION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Polyvinyl Alcohol, Acrylic Copolymer

Questions or Comments?

OTC - QUESTIONS SECTION

CALL: 1-800-PEDIFIX (733-4349)

Package LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68927-379268927-3792-1

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
NameUNIIKind
SALICYLIC ACIDO414PZ4LPZACTIB
ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S)1PEZ3NLY6IIACT
POLYVINYL ALCOHOL, UNSPECIFIED532B59J990IACT
BROWN IRON OXIDE1N032N7MFOIACT

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
8383afb5-58cd-bc55-e053-2a91aa0ae08d8383afb5-58cc-bc55-e053-2a91aa0ae08d2019-03-28WarningsExact identifier
spl id: 8383afb5-58cd-bc55-e053-2a91aa0ae08d
spl set id: 8383afb5-58cc-bc55-e053-2a91aa0ae08d

Reported adverse events (FAERS/openFDA)#

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