MICONAZOLE NITRATE- antifungal miconazorb af powder talc free powder

Miconazole nitrate by

Drug Labeling and Warnings

Miconazole nitrate by is a Otc medication manufactured, distributed, or labeled by Family Dollar Services Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Miconazole nitrate 2%

Purpose

Antifungal

Uses

for the cure of most athlete's foot, jock itch and ringworm

Warnings

For external use only.

Do not use

on children under 2 years of age unless directed by a doctor.

When using this product

avoid contact with the eyes

Stop use and ask a doctor if

irritation occurs or 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

• clean the affected area & dry thoroughly
• apply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor
• 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, & change shoes & socks at least once daily
• for athlete's foot & ringworm, use daily for 4 weeks; for jock itch, use daily for 2 weeks
• if condition persists longer, consult a doctor
• this product is not effective on the scalp or nails

Other information

• store between 59º - 86ºF
• lightly shake bottle to loosen settled powder

Inactive ingredients

allantoin, chloroxylenol, fragrance, imidazolidinyl urea, microcrystalline cellulose, tricalcium phosphate, zea mays (corn) starch

Questions?

Call 1-866-964-0939

Pincipal Display Panel

FAMILY Wellness

Antifungal

Miconazorb AF

Powder

Miconazole Nitrate 2%

Talc-Free

• Cures most athlete's foot, jock itch & ringworm
• Relieves chafing, itching, burning & scaling
• Absorbs moisture

Net wt 2.5 OZ (71 g)

INGREDIENTS AND APPEARANCE

MICONAZOLE NITRATE 
antifungal miconazorb af powder talc free powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55319-144
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M)	MICONAZOLE NITRATE	1.42 g  in 71 g

Inactive Ingredients
Ingredient Name	Strength
ZEA MAYS SUBSP. MAYS WHOLE (UNII: 1G5HNE09V8)
ALLANTOIN (UNII: 344S277G0Z)
IMIDUREA (UNII: M629807ATL)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
TRICALCIUM PHOSPHATE (UNII: K4C08XP666)
CHLOROXYLENOL (UNII: 0F32U78V2Q)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55319-144-71	71 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/01/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333C	10/01/2019

Labeler - Family Dollar Services Inc. (024472631)