Leader Medicated description, usages, side effects, indications, overdosage, supplying and lots more!

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Leader Medicated

Cardinal Health Inc.
Premier Brands of America

Drug Facts




FULL PRESCRIBING INFORMATION

Tolnaftate 1%

Antifungal

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

Uses

  • cures most athlete's foot (tinea pedis), ringworm (tinea corporis) and jock itch (tinea cruris)
  • if used daily, can prvent recurrance of athlete's foot
  • relieves symptoms 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 120o F

  • do not get into eyes or mouth
  • use only as directed; intentional misuse by deliberately concentrating and inhaling contents can be harmful or fatal
  • irritation occurs
  • no improvement after four weeks for athlete's foot,
  • wash affected area and dry thoroughly
  • shake can well and spray 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 toes, wear well-fitting, ventilated shoes and change shoes and socks at least once daily
  • use daily for 4 weeks for athlete's foot and ringworm; use daily for 2 weeks for jock itch, if condition persists, consult a doctor
  • to prevent athlete's foot, apply daily (morning and night)
  • this product is not effective on scalp or nails
  • in case of clogging, clear nozzle under running water

Store between 20o and 30o C (68o and 86o F)

SD alcohol 40-B (14% w/w), BHT, Isobutane (propellant), PPG-12-buteth-16, talc

Call 1-866-964-0939

Leader MedicatedLeader Medicated Tolnaftate 1% Powder Spray

Leader Medicated

TOLNAFTATE AEROSOL, POWDER

Product Information

Product Type Human otc drug label Item Code (Source) NDC:37205-344
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
ALCOHOL
isobutane
PPG-12-buteth-16
talc

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:37205-344-66 130 in 1 CAN

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partC part333C 2008-03-15


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Be sure to consult your doctor before taking any medication!
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