MOSCO- salicylic acid liquid

MOSCO by

Drug Labeling and Warnings

MOSCO by is a Otc medication manufactured, distributed, or labeled by Medtech Products Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Salicylic Acid 17.6%

Purpose

Callus & corn remover

Use

For removal of calluses and corns

Warnings

For external use only

• Extremely flammable
• Keep away from fire or flame. Avoid smoking during use and until product has dried.
• Cap bottle tightly after each use and store at room temperature away from heat.
• Avoid inhaling vapors.
• If product gets into the eye, flush with water for 15 minutes.

Do not use:

• on irritated skin
• on any area that is reddened or infected

Ask a doctor before use if you have:

• diabetes
• poor blood circulation
• if you have diabetes or poor blood circulation

Stop use and ask a doctor

if discomfort persists

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

• Wash affected area
• Dry thoroughly
• Apply one drop at a time to sufficiently cover each callus and corn
• Let dry
• Repeat this procedure once or twice daily as needed for up to 14 days (or until callus or corn is removed)
• You may soak callus or corn in warm water for 5 minutes to assist removal.

Other information

• Store at room temperature
• Avoid excessive heat

Inactive ingredients

alcohol, ether

Questions?

1-800-443-4908

PRINCIPAL DISPLAY PANEL

MOSCO Liquid Callus & Corn Remover 0.31 mL (9 mL)

INGREDIENTS AND APPEARANCE

MOSCO 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63029-309
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	150 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
ETHER (UNII: 0F5N573A2Y)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63029-309-03	1 in 1 CARTON	10/01/1999
1		9 mL in 1 BOTTLE, GLASS; 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	10/01/1999

Labeler - Medtech Products Inc. (122715688)