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

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Kendall Antifungal

COVIDIEN INC.

Kendall Antifungal Cream




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredient

Miconazole nitrate 2%

Purpose

Purpose

Antifungal

Uses

Uses

  • for the treatment of most athlete's foot (tinea pedis), jock itch (tinea cruris), and ringworm (tinea corporis).
  • for effective relief of itching, scaling, cracking, burning, redness, soreness, irritation, discomfort, and chafing associated with jock itch.

Warnings

Do not use on children under two years old unless directed by a doctor.

For external use only.

When using this product
  • do not get into eyes
For the treatment of athlete's foot and ringworm,


For the treatment of jock itch,


Keep out of the reach of children.



Directions  Clean the affected area and dry thoroughly.  Apply a thin layer of the product over the 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 four weeks; for jock itch, use daily for two weeks.  If condition persists longer, consult a doctor.  This product is not effective on the scalp or nails.

Other Information

  • protect from freezing
  • avoid excessive heat

Inactive ingredients

Water, mineral oil propylene glycol, sorbitane stearate, cetyl alcohol, isopropyl palmitate, simmondsia chinensis (jojoba) seed oil, sodium lactate, polysorbate 60, dimethicone, butyrospermum parkii (shea butter), decylene glycol, xanthan gum, retinyl palmitate, tocopheryl acetate, cetyl hydroxyethylcellulose, methylparaben, propylparaben, diazolidinyl urea

Questions or comments?  1-800-962-9888


Image of Antifungal Cream 4 oz Label

Kendall Antifungal

Kendall Antifungal

Miconazole nitrate CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:28851-692
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MICONAZOLE NITRATE MICONAZOLE 2 g

Inactive Ingredients

Ingredient Name Strength
water
Mineral Oil
propylene glycol
SORBITAN MONOSTEARATE
CETYL ALCOHOL
ISOPROPYL PALMITATE
sodium lactate
Jojoba Oil
POLYSORBATE 60
VITAMIN A PALMITATE
DIMETHICONE
SHEA BUTTER
CETYL HYDROXYETHYLCELLULOSE (350000 MW)
METHYLPARABEN
1-DECENE
PROPYLPARABEN
DIAZOLIDINYL UREA
XANTHAN GUM
ALPHA-TOCOPHEROL ACETATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:28851-692-01 118 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partC part333C 2011-04-14


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Be sure to consult your doctor before taking any medication!
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