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Lamisil AT Continuous Spray

Generic Name: terbinafine hydrochloride
Dosage Form: liquid

Drug Facts

Active ingredient

Terbinafine hydrochloride

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Purpose

Antifungal

Uses

  • cures most jock itch (tinea cruris)
  • relieves itching, burning, cracking, and scaling which accompany this condition

Warnings

For external use only

Do Not Use

  • on nails or scalp
  • in or near the mouth or the eyes
  • for vaginal yeast infections

When using this product

do not get into eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor

if too much irritation occurs or gets worse.

Keep Out of Reach of Children

If swallowed, get medical help or contact a Poison Control

Center right away.  

Directions

  • adults and children 12 years and over
    • wash the affected area with soap and water and dry completely before applying
    • to open remove clear cap.
    • hold can 4" to 6" from skin.  Press and hold to spray a thin layer over affected area
    • spray affected area once a day (morning or night) for 1 week or as directed by a doctor
    • release to stop spray
    • wipe excess from spray opening after each use
    • return cap to can
    • wash hands after each use
  • children under 12 years: ask a doctor

Other information

store at 8° - 25° C (46° - 77° F)

Additional Information

Full Prescription Strength

Continuous Spray Action

Cures Most Jock Itch

For Effective Relief of Itching & Burning

Distr. By:  

 
Novartis Consumer Health, Inc.
 
Parsippany, NJ 07054-0622 ©2009

Inactive ingredients

Ethanol, polyoxyl 20 cetostearyl ether, propylene glycol, purified water

Questions

call 1-800-452-0051 or visit us at www.lamisilat.com

Principal Display

LAMISIL  AT CONTINUOUS SPRAY
terbinafine hydrochloride liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0067-6293
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TERBINAFINE HYDROCHLORIDE (TERBINAFINE) TERBINAFINE HYDROCHLORIDE 1.25 mL  in 125 mL
Inactive Ingredients
Ingredient Name Strength
ALCOHOL  
POLYOXYL 20 CETOSTEARYL ETHER  
PROPYLENE GLYCOL  
WATER  
Packaging
# Item Code Package Description
1 NDC:0067-6293-83 125 mL in 1 BOTTLE, SPRAY
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA021124 07/23/2009
Labeler - Novartis Consumer Health, Inc. (879821635)
Revised: 01/2010
 
Novartis Consumer Health, Inc.



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