Kiss Fungi-Gone description, usages, side effects, indications, overdosage, supplying and lots more!

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Kiss Fungi-Gone

Kiss Products, Inc.

Kiss Fungi-Gone Antifungal Treatment - Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredient

Tolnaftate 1%

Purpose

Anti-fungal

Kiss Fungi-Gone Uses

For the cure of:

  • athlete's foot (tinea pedis)
  • jock itch (tinea cruris)
  • ringworm (tinea corporis)

For the relief of:

  • itching
  • cracking
  • burning
  • scaling
  • discomfort associated with the above condition

Warnings

For external use only. Avoid contact with eyes.

Do not use

  • for bacterial infections
  • for diaper rash
  • on children under 2 years of age unless directed by a doctor

Do not use and ask doctor if:

  • irritation occurs
  • there is no improvement within 4 weeks

KEEP OUT OF REACH OF CHILDREN.

In case of accidental ingestion, get medical help or contact Poison
Control Center right away. As with any drug, if pregnant or nursing a baby, consult with a doctor before using.

Directions

  • Shake well before using
  • Clean area with soap and water, dry thoroughly
  • Apply thin layer over affected area 2 times a day
  • For athlete's foot, use daily for 4 weeks or as directed by a physician
  • Allow solution to soak into the skin before putting socks on
  • This product is not effective on nails and scalp

Other Information

This product contains Acetone. Do not use near heat or flame.

Inactive Ingredients

Acetone, Water, Propylene Glycol, Polysorbate 80, Undecylenic Acid, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate (Vitamin E)

Image of Labels and Cartons

FungiGoneHalfOunceLabel.jpgKiss Fungi-Gone FungiGoneHalfOunceCarton.jpgKiss Fungi-Gone FungiGoneOneOunceLabel.jpgKiss Fungi-Gone FungiGoneOneOunceCarton1.jpgKiss Fungi-Gone FungiGoneOneOunceCarton2.jpgKiss Fungi-Gone

Kiss Fungi-Gone

Tolnaftate LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:42432-019
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
acetone
propylene glycol
water
polysorbate 80
UNDECYLENIC ACID
Aloe Vera Leaf
ALPHA-TOCOPHEROL ACETATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:42432-019-03 15 in 1 BOTTLE, WITH APPLICATOR
2 NDC:42432-019-05 30 in 1 BOTTLE, WITH APPLICATOR
3 NDC:42432-019-06 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partC part333C 2012-10-23


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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