WARRIOR ANTIFUNGAL FOOT- miconazole nitrate 2% powder

Warrior Antifungal Foot by

Drug Labeling and Warnings

Warrior Antifungal Foot by is a Otc medication manufactured, distributed, or labeled by Derma Care Research Labs, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Miconazole Nitrate 2%

PURPOSE

Antifungal

INDICATIONS & USAGE

For the cure of athlete's foot and jock itch. Relieves itching and chafing associated with jock itch.

WARNINGS

For external use only. Do not use on children under 2 years of age unless directed by a doctor or for diaper rash. When using thisproduct avoid contact with the eyes. Stop use and ask a doctor if irritation occurs or if 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.

DOSAGE & ADMINISTRATION

Cleanse the affected area and dry thoroughly. Apply a thin layer of the product over the affected area twice daily or as directed by a doctor or healthcare professional. Supervise children in the use of this product.

For athlete's foot: pay special attention to space between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily. Use daily for 4 weeks.

If the condition persists, consult a doctor.

This product is not effective on the scalp or nails.

INACTIVE INGREDIENT

Corn Starch, Fragrance, Potassium Sorbate, Rice Starch, Sodium Benzoate.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WARRIOR ANTIFUNGAL FOOT 
miconazole nitrate 2% powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72839-961
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M)	MICONAZOLE NITRATE	2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
SODIUM BENZOATE (UNII: OJ245FE5EU)
STARCH, CORN (UNII: O8232NY3SJ)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
STARCH, RICE (UNII: 4DGK8B7I3S)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72839-961-02	71 g in 1 BOTTLE; Type 0: Not a Combination Product	02/02/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333C	02/02/2021

Labeler - Derma Care Research Labs, LLC (116817470)

Registrant - Derma Care Research Labs, LLC (116817470)

Establishment
Name	Address	ID/FEI	Business Operations
Derma Care Research Labs, LLC		116817470	manufacture(72839-961)