ONGO - FIN- tolnaftate liquid

Ongo - Fin by

Drug Labeling and Warnings

Ongo - Fin by is a Otc medication manufactured, distributed, or labeled by Efficient Laboratories Inc., Dextrum Laboratories Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients:

Tolnaftate 1% v/v........Antifungal

PURPOSE

Uses:

For effective treatment of Athlete's Foot (tinea pedis). For the relieve if itching, burning feet.

Treatment for ringworm (tinea corporis). For the prevention of athlete's foot with daily use.

WARNINGS

Warnings:

Do not use on children under 2 years of age. Do not use for diaper rash. For external use only. Do not use if safety seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN

Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away. Flammable. Keep away from fire and flame.

DOSAGE & ADMINISTRATION

Directions:

• Clean the affected area with soap and water, dry thoroughly.
• Apply a thin layer of Ongo Fin over the affected area twice daily (morning and night) or as directed by a physician.
• 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.
• For more effective results, continue applying Ongo Fin for 2 more weeks after the symptoms have disappeared.
• Supervise children in the use if this product.
• Ongo Fin is not effective on scalp or nails
• Store between 15 - 30 degrees celcius ( 59 - 86 degrees farhenheit).
  

INDICATIONS & USAGE

When using this product, avoid contact with eyes. Stop use and consult a doctor if irritation occurs or if there is no improvement within 4 weeks.

INACTIVE INGREDIENT

Inactive Ingredients:

Acetone, Aloe Vera Gel, Propylene Glycol, Purified Water and Tocopheryl Acetate (Vitamin E).

QUESTIONS

Distributed By:

Effecient laboratories, Inc.
Miami FL 33166

www.efficientlab.com

(305) 805-3456  Monday to Friday 

9:00am - 5:00pm EST

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ONGO - FIN 
tolnaftate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58593-800
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV)	TOLNAFTATE	1 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ACETONE (UNII: 1364PS73AF)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58593-800-01	30 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	02/01/2004
2	NDC: 58593-800-02	30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	02/01/2004

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333C	02/01/2004

Labeler - Efficient Laboratories Inc. (969044932)