Novana Antifungal Barrier with Miconazole description, usages, side effects, indications, overdosage, supplying and lots more!

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Novana Antifungal Barrier with Miconazole

Novana Medical, LLC
O.L. PRODUCTS, INC.

Drug Facts




FULL PRESCRIBING INFORMATION

Active ingredient

Active ingredient                       Purpose
Miconazole Nitrate 2%..............Antifungal

Purpose

Indications For effective treatment of athlete's foot (dermatophytosis), jock itch (tinea cruris), and ringworm (tinea corporis). • For the relief of burning, redness, irritation, discomfort, itching, scaling, and cracking.

Warnings 

For external use only. 

Do not use on children under 2 years of age unless directed by a doctor. Avoid contact with the eyes • If irritation occurs or if there is no improvement within 4 weeks, discontinue use and consult a doctor.

Keep this and all drugs out of the reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

Uses

Directions  • Clean the affected area and 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, and change shoes and socks at least once daily. For athlete's foot and 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.

Use Daily for 2 weeks.
If condition persists, consult a doctor. This product is not effective on scalp or nails.

Inactive ingredients
Cetyl Alcohol,Cod Liver Oil, Diazolidinyl Urea, Dimethicone, Glyceryl Stearate, Lanolin Oil, Methylparaben, Petrolatum, Propanediol, Propylene Glycol, Propylparaben, Sodium Laureth Sulfate, Water, Zinc Oxide


Novana Antifungal Barrier with Miconazole

Novana Antifungal Barrier with Miconazole

Miconazole Nitrate CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:76077-400
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MICONAZOLE NITRATE MICONAZOLE .02 mL

Inactive Ingredients

Ingredient Name Strength
water
CETYL ALCOHOL
GLYCERYL MONOSTEARATE
petrolatum
LANOLIN
COD LIVER OIL
PROPANEDIOL
SODIUM LAURETH SULFATE
propylene glycol
DIAZOLIDINYL UREA
METHYLPARABEN
PROPYLPARABEN
Zinc Oxide
DIMETHICONE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:76077-400-04 120 in 1 TUBE
2 NDC:76077-400-07 210 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partC part333C 2012-04-04


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Be sure to consult your doctor before taking any medication!
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