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Tinactin

MSD Consumer Care, Inc.

Tinactin


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Tolnaftate 1%

Purpose

Antifungal

Tinactin Uses

  • proven clinically effective in the treatment of most athlete's foot (tinea pedis) and ringworm (tinea corporis)
  • helps prevent most athlete's foot with daily use
  • for effective relief of itching, burning and cracking

Warnings

For external use only

Avoid contact with the eyes

Stop use and ask a doctor if

  • irritation occurs
  • there is no improvement within 4 weeks

Do not use on children under 2 years of age except under the advice and supervision of 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
  • apply 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
  • use daily for 4 weeks; if condition persists longer, ask a doctor
  • to prevent athlete's foot, apply once or twice daily (morning and/or night)
  • this product is not effective on the scalp or nails

Tinactin Other information

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

Inactive ingredients

benzethonium chloride, corn starch, kaolin, sodium bicarbonate

Questions?

1-866-360-3266

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 - 108g Can Label

NDC 11523-0444-2

TOUGH ACTIN' ®
Tinactin ®

ANTIFUNGAL
tolnaftate

Cures and
prevents most
athlete's foot

SUPER ABSORBENT
POWDER

Relieves itching
& burning

NET WT 108g (3.8 oz)

Tinactin

Tinactin

Tolnaftate POWDER

Product Information

Product Type Human otc drug label Item Code (Source) NDC:11523-0444
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Tolnaftate TOLNAFTATE 10 mg

Inactive Ingredients

Ingredient Name Strength
benzethonium chloride
STARCH, CORN
KAOLIN
SODIUM BICARBONATE

Product Characteristics

Color
WHITE (white to off-white)

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:11523-0444-2 108 in 1 CAN

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partC part333C 1993-09-23


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Be sure to consult your doctor before taking any medication!
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