Baza Antifungal description, usages, side effects, indications, overdosage, supplying and lots more!

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Baza Antifungal

Coloplast Manufacturing US, LLC
Coloplast Corp

AntifungalMoisture BarrierAntifungalCream




FULL PRESCRIBING INFORMATION

For Perineal
Skin Irritation Due to
Fungal Infection

Drug Facts

Active ingredient

Active ingredient

Miconazole Nitrate, 2%

Purpose

Purpose

Antifungal

Uses

Uses For effective treatment of jock itch. Relieves itching, scaling, irritation, redness and discomfort.

Warnings

When using this product

  • avoid contact with eyes
  • do not use on children under 2 years of age unless directed by a doctor.

Stop using this product and ask a doctor if irritation occurs or there is no improvement within 2 weeks.

For external use only.

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

Directions

  • clean the affected area and dry thoroughly
  • apply thin layer of product over affected area twice daily (morning and night), or as directed by a doctor
  • supervise children in the use of this product.

Use daily for 2 weeks.

If condition persists, consult a doctor. This product is not effective on scalp or nails.

Inactive ingredients

BHT, cetearth-6, cetyl alcohol, cod liver oil, diazolidinyl urea, fragrance, glyceryl stearate, lanolin oil, PEG-100 stearate, petrolatum, polmethoxybicyclic oxazolidine, propylene glycol, water, stearyl alcohol, tocopheryl acetate, zinc oxide

See crimp for lot no. and expiration date

Manufactured by: Coloplast A/S DK-3050 Humlebaek, Denmark
Distributed by: Coloplast Corp. Minneapolis, MN 55411 U.S.A.
1-800-533-0464 www.us.coloplast.com
Product #1607 ©2008-7, Coloplast Corp.
Made in the U.S.A.

G8-664

PRINCIPAL DISPLAY PANEL - NET WT. 5 OZ. (142 g)

NDC 11701-045-14

Baza ® Antifungal

Antifungal

Moisture Barrier Antifungal Cream

For Perineal Skin Irritation Due to Fungal Infection

Coloplast

NET WT. 5 OZ. (142 g)

Baza Antifungal

Miconazole nitrate CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:11701-045
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MICONAZOLE NITRATE MICONAZOLE 20 mg

Inactive Ingredients

Ingredient Name Strength
petrolatum
CETYL ALCOHOL
GLYCERYL MONOSTEARATE
BUTYLATED HYDROXYTOLUENE
COD LIVER OIL
.ALPHA.-TOCOPHEROL ACETATE, D-
LANOLIN
CETEARETH-6
stearyl alcohol
propylene glycol
PEG-100 STEARATE
Zinc Oxide
DIAZOLIDINYL UREA
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:11701-045-22 4 in 1 PACKET
2 NDC:11701-045-23 57 in 1 TUBE
3 NDC:11701-045-14 142 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partC part333C 2009-06-15


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Be sure to consult your doctor before taking any medication!
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