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jock itch

WALGREEN COMPANY

Walgreen Co. Jock Itch Powder Spray Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Tolnaftate 1%

Purpose

Antifungal

jock itch Uses

  • proven clinically effective in the treatment of most jock itch (tinea cruris)
  • effectively soothes and relieves symptoms of jock itch
  • itching
  • chafing
  • burning

Warnings

For external use only

Flammable: Do not use near flame or spark or while smoking.

Do not use

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

When using this product

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

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.

Directions

  • clean the affected area and dry thoroughly
  • shake can well before use
  • hold can about 6 inches from the area to be treated
  • spray a thin layer over the affected area twice daily (morning and night)
  • supervise children in the use of this product
  • use daily for 2 weeks. If condition lasts longer, ask a doctor.
  • this product is not effective on the scalp or nails
  • in case of clogging, clean nozzle with a pin

Inactive ingredients

alcohol SD 40-B, aluminum starch octenylsuccinate, isobutane, isopropyl myristate, propane, propylene carbonate, sorbitan monooleate, stearalkonium hectorite, talc

Questions or comments?

1-800-719-9260

Package/Label Principal Display Panel

Compare to Tinactin® active ingredient

MAXIMUM STRENGTH

JOCK ITCH POWDER SPRAY

Tolnaftate 1%

Antifungal

Cures Most Jock Itch

Soothes and Relieves Itching, Burning and Chafing

jock itch
Jock Itch Powder Spray Label

jock itch

Tolnaftate SPRAY

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0363-0695
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Tolnaftate TOLNAFTATE 1 g

Inactive Ingredients

Ingredient Name Strength
ALUMINUM STARCH OCTENYLSUCCINATE
isobutane
ISOPROPYL MYRISTATE
propane
PROPYLENE CARBONATE
SORBITAN MONOOLEATE
talc

Product Characteristics

Color
WHITE (off-white)

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0363-0695-90 130 in 1 CAN

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partC part333C 2005-06-08


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Be sure to consult your doctor before taking any medication!
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