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Tolnaftate

CVS Pharmacy

Medicated Antifungal Continuous Liquid Spray




FULL PRESCRIBING INFORMATION

Tolnaftate 1%

Antifungal

  • cures most athlete's foot (tinea pedis) and ringworm (tinea corporis)
  • if used daily, can prevent recurrence of athlete's foot
  • relieves sypmtoms of athlete's foot, including itching, burning and cracking

For external use only.

Do not use while smoking or near heat or flame. Do not puncture or incinerate. Contents under pressure. Do not store at temperature above 120ºF

  • do no get into eyes or mouth
  • use only as directed

Intentional misuse by deliberately concentrating and inhaling contents cans be harmful or fatal.

  • irritation occurs
  • no improvement within 4 weeks

If swallowed, get medical help or contact a Poison Control Center right away. Do not use on children under 2 years of age unless directed by a doctor.

  • wash affected area and dry thoroughly
  • shake can well and spray a thin layer over 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
  • use daily for 4 weeks: if conditions persist, consult 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

store between 20º and 30ºC (68ºF and 86º)

BHT, PPG-12-buteth-16, SD alcohol 40-B(80%w/w)

call 1-866-964-0939

Medicated Antifungal Continuous Liquid Spray
Tolnaftate 1%

  • Cures & prevents most athlete's foot
  • Relieves itching & burning

NET WT 5.3oz(150g)

Tolnaftate

Tolnaftate

Antifungal Continuous Liquid Spray AEROSOL, SPRAY

Product Information

Product Type Human otc drug label Item Code (Source) NDC:59779-572
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Tolnaftate TOLNAFTATE 1.5 g

Inactive Ingredients

Ingredient Name Strength
ALCOHOL
BUTYLATED HYDROXYTOLUENE
PPG-12-buteth-16

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:59779-572-53 150 in 1 CAN

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partC part333C 2014-01-01


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