MEDIPLAST- salicylic acid plaster 
Medline Industries, Inc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredient

40% Salicylic Acid

Purpose

Corn, Callus, and Wart Remover

Uses

For the removal of

Warnings

For external use only. This product contains natural rubber, which may cause allergic reactions.

Do not use

  • if you are diabetic or have poor blood circulation
  • on irritated skin or on any area that is infected or reddened
  • on moles, birthmarks, or warts with hair growing from them, genital warts, warts on the face, warts on mucous membranes such as warts inside the mouth, nose, anus, genitals or lips.

Keep this and all drugs out of reach of children.

In case of accidental ingestion, seek professional assistance or contact a Poison Control center immediately.

Stop using this product and see your doctor

if discomfort persists.

Directions

Wash affected area. May soak corn, callus or wart in warm water for 5 minutes. Dry area thoroughly. Cut pad to fit corn, callus or wart. Apply medicated pad to area. Remove medicated pad after 48 hours. Repeat procedure every 48 hours for up to 14 days for corn/callus removal and up to 12 weeks for warts, until the problem has cleared.

Inactive ingredients

O-Cresol, Lanolin, Myroxylon pereirae (Balsam Peru), Phenol, Talc, Terpineol.

Bandage: Flannel (99.7% cotton), Colophonium, Rubber Latex, 0.3% Polyurethane

Package/Label Principal Display Panel

Mediplast Corn, Callus & Wart Remover Packet Principal Display Panel

NDC: 53329-410-09

CURAD

WE HELP HEAL

MEDIPLAST

Corn, Callus & Wart Remover

Made in Germany

Distributed by Medline Industries, Inc. Mundelein, IL 60060

This Product Contains Dry Natural Rubber

Package Label/Drug Facts

Mediplast Corn, Callus & Wart Remover Packet Drug Facts

Box Label / Principal Display Panel

Box Label / Principal Display Panel

Box Label / Back and Top

Box Label / Top and Back
MEDIPLAST 
salicylic acid plaster
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:53329-410
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 40 g  in 100 g
Inactive Ingredients
Ingredient Name Strength
LANOLIN (UNII: 7EV65EAW6H)  
NATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN)  
BALSAM PERU (UNII: 8P5F881OCY)  
ROSIN (UNII: 88S87KL877)  
TALC (UNII: 7SEV7J4R1U)  
TERPINEOL (UNII: R53Q4ZWC99)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:53329-410-59 25 in 1 BOX
1 NDC:53329-410-09 1 in 1 PACKET
1 1.4 g in 1 APPLICATOR
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part358F 08/01/2008
Labeler - Medline Industries, Inc (025460908)

Revised: 11/2012
Document Id: a925113e-347e-4051-b092-f947b8252d74
Set id: 35bd29f9-cf49-404b-826b-72d1269d4f19
Version: 3
Effective Time: 20121130
 
Medline Industries, Inc