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sunmark

McKesson
Taro Pharmaceuticals U.S.A., Inc.

sunmark antifungal


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Tolnaftate 1%

Purpose

Antifungal

sunmark Uses

  • clinically proven to cure most athlete's foot (tinea pedis), jock itch (tinea cruris) and ringworm (tinea corporis)
  • helps prevent most athlete's foot from recurring when used daily
  • effectively soothes and relieves symptoms of athlete's foot, including itching, burning and cracking

Warnings

For external use only

When using this product avoid contact with the eyes

Stop use and ask a doctor if

  • irritation occurs
  • there is no improvement within 4 weeks (for athlete's foot or ringworm) or within 2 weeks (for jock itch)

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
  • this product is not effective on scalp or nails

For athlete's foot

  • pay special attention to spaces between toes
  • wear well-fitting shoes, 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

sunmark Other information

  • Store between 15° - 30°C (59° - 86°F)
  • See end panel of carton and tube crimp for lot number and expiration date

Inactive ingredients

BHT, PEG-400, PEG-3350, titanium dioxide, white petrolatum

Distributed by McKesson
One Post Street
San Francisco, CA 94104

PRINCIPAL DISPLAY PANEL - 15 g Tube Carton

sunmark

antifungal cream

Tolnaftate 1%
CURES & PREVENTS MOST ATHLETE'S FOOT

NET WT 0.5 OZ (15 g)

sunmark

sunmark

Tolnaftate CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:49348-155
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
BUTYLATED HYDROXYTOLUENE
polyethylene glycol 400
POLYETHYLENE GLYCOL 3350
titanium dioxide
petrolatum

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 15 in 1 TUBE
2 NDC:49348-155-29 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partC part333C 2006-02-17


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Be sure to consult your doctor before taking any medication!
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