Quinsana Anti-Fungal Powder 2% Miconazole Nitrate

Quinsana Anti-Fungal Powder 2 Miconazole Nitrate by

Drug Labeling and Warnings

Quinsana Anti-Fungal Powder 2 Miconazole Nitrate by is a Otc medication manufactured, distributed, or labeled by Profoot Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

QUINSANA ANTI-FUNGAL POWDER 2 MICONAZOLE NITRATE- miconazole nitrate powder 
Profoot Inc.

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Quinsana Anti-Fungal Powder 2% Miconazole Nitrate

Drug Facts

Active Ingredient

Miconazole Nitrate, 2%

Purpose

Antifungal

Uses

• Cures most athlete’s foot and ringworm
• Effectively relieves itching, cracking, and burning

Warnings

• For external use only

Ask a doctor before use

• on children under 2 years of age

When using this product

• avoid contact with eyes

Stop use and ask a doctor if

• irritation occurs 
• there is no improvement within 4 weeks

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Wash affected area and dry thoroughly.
• Apply a thin layer of the product over affected area twice daily (morning and night). 
• Supervise children in the use of this product. 
• For athlete’s foot: pay special attention to spaces between the toes. Wear well-fitting, ventilated shoes, and change shoes and socks at least once daily. 
• Use daily for 4 weeks; if condition persists longer, ask a doctor. 
• This product is not effective on the scalp or nails.

Inactive ingredients

Zea Mays (Corn) Starch, Tricalcium Phosphate, Microcrystalline Cellulose, Allantoin, Imidazolidinyl Urea, Chloroxylenol, Fragrance.

Package Labeling:

QUINSANA ANTI-FUNGAL POWDER 2 MICONAZOLE NITRATE 
miconazole nitrate powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 29784-145
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M)	MICONAZOLE NITRATE	20 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
STARCH, CORN (UNII: O8232NY3SJ)
TRICALCIUM PHOSPHATE (UNII: K4C08XP666)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
ALLANTOIN (UNII: 344S277G0Z)
IMIDUREA (UNII: M629807ATL)
CHLOROXYLENOL (UNII: 0F32U78V2Q)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 29784-145-85	85 g in 1 BOTTLE; Type 0: Not a Combination Product	03/01/2022	12/17/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	03/01/2022	12/17/2023

Labeler - Profoot Inc. (107570900)

Revised: 11/2023

Document Id: 09bd9ee6-c422-c415-e063-6394a90ac616

34390-5

Set id: 274b427f-a2c0-4967-a3bf-07ff07eecc80

Version: 3

Effective Time: 20231109

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