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Lotrimin

MSD Consumer Care, Inc.

Lotrimin Antifungal


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Miconazole nitrate 2%

Purpose

Antifungal

Lotrimin Uses

  • Cures most athlete's foot (tinea pedis), jock itch (tinea cruris) and ringworm (tinea corporis)
  • relieves itching, cracking, burning and scaling

Warnings

For external use only

Avoid contact with the eyes

Stop use and ask a doctor if irritation occurs or if there is no improvement within 4 weeks (for athlete's foot and ringworm) or 2 weeks (for jock itch)

Do not use on children under 2 years of age unless directed by a doctor.

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

Directions

  • wash affected area and dry thoroughly
  • sprinkle a thin layer over affected area twice daily (morning and night)
  • 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, ask a doctor
  • this product is not effective on the scalp or nails

Lotrimin Other information

store between 20° to 25°C (68° to 77°F)

Inactive ingredients

benzethonium chloride, corn starch, kaolin, sodium bicarbonate, starch/acrylates/acrylamide copolymer, zinc oxide

© Copyright & Distributed by MSD Consumer Care, Inc.,
PO Box 377, Memphis, TN 38151 USA, a subsidiary of
Merck & Co., Inc., Whitehouse Station, NJ USA.

PRINCIPAL DISPLAY PANEL - 90g Can Label

NDC 11523-0919-1

LOTRIMIN ® AF
ANTIFUNGAL
miconazole nitrate

Cures Most
Athlete's Foot

POWDER

  • Absorbs Moisture
  • Relieves Itching,
    Burning & Scaling

NET WT 90g (3 OZ)

37871-00

Lotrimin

Lotrimin

Miconazole nitrate POWDER

Product Information

Product Type Human otc drug label Item Code (Source) NDC:11523-0919
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
benzethonium chloride
STARCH, CORN
KAOLIN
SODIUM BICARBONATE
Zinc Oxide

Product Characteristics

Color
WHITE (White to off-white)

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:11523-0919-1 90 in 1 CAN

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partC part333C 1993-09-01


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