MEDIPLAST- salicylic acid plaster

MediPlast by

Drug Labeling and Warnings

MediPlast by is a Otc medication manufactured, distributed, or labeled by Medline Industries, LP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

40% Salicylic Acid

Purpose

Corn, Callus, and Wart Remover

Uses

• for the removal of corns and calluses
• Relieves pain by removing corns and calluses
• for the removal of common warts. The common wart is easily recognized by the rough ‘cauliflower-like’ appearance of the surface
• for the removal of plantar warts on the bottom of the foot. 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

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

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 for more than 72 hours

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.

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 Labels

INGREDIENTS AND APPEARANCE

MEDIPLAST 
salicylic acid plaster

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53329-410
Route of Administration	TOPICAL

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
PHENOL (UNII: 339NCG44TV)
LANOLIN (UNII: 7EV65EAW6H)
NATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN)
BALSAM PERU (UNII: 8P5F881OCY)
ROSIN (UNII: 88S87KL877)
TALC (UNII: 7SEV7J4R1U)
TERPINEOL (UNII: R53Q4ZWC99)
ORTHOCRESOL (UNII: YW84DH5I7U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53329-410-59	25 in 1 BOX	08/01/2008
1	NDC: 53329-410-09	1 in 1 PACKET
1		1.4 g in 1 APPLICATOR; Type 0: Not a Combination Product

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)

Establishment
Name	Address	ID/FEI	Business Operations
Strukmyer Medical		078587210	manufacture(53329-410)