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LAMISIL AT by Novartis Consumer Health, Inc.

Medically reviewed on January 1, 2018

Dosage form: spray
Ingredients: TERBINAFINE HYDROCHLORIDE 1mL in 100mL
Labeler: Novartis Consumer Health, Inc.
NDC Code: 0067-4000

Drug Facts

Active ingredient

Terbinafine hydrochloride

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
    • spray affected area once a day (morning or night) for 1 week or as directed by a doctor
    • 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

For Effective Relief of: ° Itching ° Burning

Distr. By:  

 
Novartis Consumer Health, Inc.
 
Parsippany, NJ 07054-0622 ©2006

Inactive ingredients

cetomacrogol, ethanol, propylene glycol, purified water USP

Questions

call 1-800-452-0051 24 hours a day, 7 days a week

Principal Display

LAMISIL AT 
terbinafine hydrochloride spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0067-4000
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TERBINAFINE HYDROCHLORIDE (TERBINAFINE) TERBINAFINE HYDROCHLORIDE1 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL 
CETETH-20 
PROPYLENE GLYCOL 
WATER 
Packaging
#Item CodePackage Description
1NDC:0067-4000-0130 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA02112405/01/2000
Labeler - Novartis Consumer Health, Inc. (879821635)

 
Novartis Consumer Health, Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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