HONGO KILLER- tolnaftate powder

Hongo Killer by

Drug Labeling and Warnings

Hongo Killer by is a Otc medication manufactured, distributed, or labeled by Efficient Laboratories Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients:             Purpose

Tolnaftate 1% W/W........................ Antifungal

INDICATIONS & USAGE

Uses

For effective treatment of:

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

For the relief of itching, burning feet.
For the prevention of athlete's foot with daily use

PURPOSE

Purpose

Antifungal

WARNINGS

Warnings

For external use only. Avoid contact with eyes.

DO NOT USE

Do not use on children under 2 years of age

Stop use and ask a doctor if irritation occurs or if there's no improvement within 4 weeks (for athlete's foot or ringworm) or within 2 weeks for jock itch.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. If pregnant or breast-feeding consult a health professional before use.

DOSAGE & ADMINISTRATION

Directions

• clean the affected area and dry thoroughly
• Sprinkle Hongo Killer powder liberally over the affected area twice daily (morning and night) or as direct by doctor
• 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 athlete's foot and ringworm, use daily for 4 weeks; for jock itch, use daily for 2 weeks. If condition persists longer, consult a doctor. This prodcut is not effective on scalp or nails.
• Supervise children in the use of Hongo Killer

QUESTIONS

Questions or comments?

www.efficientlabs.com

Please Call 305-805-3456 (M-F 9:00-5:00 pm EST)

INACTIVE INGREDIENT

Inactive ingredients Corn (Zea Mays) Starch, Methylparaben, Propylparaben, Sodium Bicardbonate, Talc and Zinc Oxide.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HONGO KILLER 
tolnaftate powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58593-288
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
STARCH, CORN (UNII: O8232NY3SJ)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
TALC (UNII: 7SEV7J4R1U)
ZINC OXIDE (UNII: SOI2LOH54Z)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58593-288-04	90 g in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2000
2	NDC: 58593-288-07	200 g in 1 BOTTLE; Type 0: Not a Combination Product	05/02/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333C	01/01/2000

Labeler - Efficient Laboratories Inc (969044932)