GOOD SENSE JOCK ITCH- tolnaftate spray

good sense jock itch by

Drug Labeling and Warnings

good sense jock itch by is a Otc medication manufactured, distributed, or labeled by L. Perrigo Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Tolnaftate 1%

Purpose

Antifungal

Uses

• cures most jock itch
• for effective relief of itching, chafing and burning

Warnings

For external use only

Flammable: Do not use while smoking or near heat or flame

Do not use

on children under 2 years of age unless directed by a doctor

When using this product

• avoid contact with the eyes
• use only as directed. Intentional misuse by deliberately concentrating and inhaling contents can be harmful or fatal.
• contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120°F (49°C).

Stop use and ask a doctor if

• irritation occurs
• there is no improvement within 2 weeks

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Directions

• 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
• use daily for 2 weeks; if condition persists longer, ask a doctor
• this product is not effective on the scalp or nails
• in case of clogging, clean nozzle with a pin

Other information

• store at 20-25°C (68-77°F)

Inactive ingredients

alcohol denat., aluminum starch octenylsuccinate, isobutane, isopropyl myristate, propylene carbonate, sorbitan monooleate, stearalkonium hectorite, talc

Questions or comments?

1-800-719-9260

Package/Label Principal Display Panel

Powder Spray

Jock Itch Spray

Antifungal

Tolnaftate 1%

Cures Most Jock Itch

Relieves Itching, Burning & Chafing

Goes on Dry

Compare to active ingredient of Tinactin® Antifungal Powder Spray

NET WT 4.6 OZ (130 g)

INGREDIENTS AND APPEARANCE

GOOD SENSE JOCK ITCH 
tolnaftate spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0113-0695
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
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
ISOBUTANE (UNII: BXR49TP611)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
TALC (UNII: 7SEV7J4R1U)
ALCOHOL (UNII: 3K9958V90M)
STEARALKONIUM HECTORITE (UNII: OLX698AH5P)

Product Characteristics
Color	WHITE (off-white)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0113-0695-90	130 g in 1 CAN; Type 0: Not a Combination Product	06/15/2005

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333C	06/15/2005

Labeler - L. Perrigo Company (006013346)