KISS FUNGI-GONE ANTI-FUNGAL TREATMENT- tolnaftate liquid

Kiss Fungi-Gone by

Drug Labeling and Warnings

Kiss Fungi-Gone by is a Otc medication manufactured, distributed, or labeled by Kiss Products, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Tolnaftate 1%

Purpose

Anti-fungal

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.jpg FungiGoneHalfOunceCarton.jpg FungiGoneOneOunceLabel.jpg FungiGoneOneOunceCarton1.jpg FungiGoneOneOunceCarton2.jpg

INGREDIENTS AND APPEARANCE

KISS FUNGI-GONE  ANTI-FUNGAL TREATMENT
tolnaftate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42432-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV)	TOLNAFTATE	10 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ACETONE (UNII: 1364PS73AF)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
UNDECYLENIC ACID (UNII: K3D86KJ24N)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42432-101-04	1 in 1 BOX
1	NDC: 42432-101-03	15 mL in 1 BOTTLE, WITH APPLICATOR
2	NDC: 42432-101-51	1 in 1 BOX
2	NDC: 42432-101-11	15 mL in 1 BOTTLE, WITH APPLICATOR
3	NDC: 42432-101-06	1 in 1 BOX
3	NDC: 42432-101-05	30 mL in 1 BOTTLE, WITH APPLICATOR

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333C	10/23/2012

Labeler - Kiss Products, Inc. (626892020)