QUINSANA ATHLETES FOOT ANTI FUNGAL- tolnaftate powder

Quinsana Athletes Foot Anti Fungal by

Drug Labeling and Warnings

Quinsana Athletes Foot Anti Fungal by is a Otc medication manufactured, distributed, or labeled by Profoot, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Tolnaftate, 1%

Purpose

Antifungal

Uses

• Cures most athlete's foot (tinea pedis), jock itch (tinea cruris), and ringworm (tinea corporis)
• 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 (for athlete's foot and ringworm) or 2 weeks (for jock itch)

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 time indicated.
• Supervise children in the use of this product. For athlete's foot and ringworm: Use twice daily (morning and night) for 4 weeks or as directed by physician. Pay special attention to spaces between the toes. Wear well-fitting, ventilated shoes, and change shoes and socks at least once daily.  For jock itch: Use daily for 2 weeks. 
• Clean the affected area and dry thoroughly.
• This product is not effective on the scalp or nails.

Inactive ingredients

Talc, Cornstarch.

Package Labeling:

INGREDIENTS AND APPEARANCE

QUINSANA ATHLETES FOOT ANTI FUNGAL 
tolnaftate powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 29784-141
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV)	TOLNAFTATE	10 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
TALC (UNII: 7SEV7J4R1U)
STARCH, CORN (UNII: O8232NY3SJ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 29784-141-85	85 g in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333C	05/01/2019

Labeler - Profoot, Inc. (107570900)