Lamisil AT Jock Itch

Dosage form: cream
Ingredients: TERBINAFINE HYDROCHLORIDE 10mg in 1g
Labeler: Novartis Consumer Health, Inc.
NDC Code: 0067-3999

Drug Facts

Active ingredient

Terbinafine hydrochloride

Purpose

Antifungal

Uses
  • cures most jock itch (tinea cruris) and ringworm (tinea corporis)
  • relieves itching, burning, cracking and scaling which accompany these conditions

Warnings

For external use only

Do not use
  • in or near the mouth or eyes
  • for vaginal yeast infections

When using this product

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

Stop Use and ask 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:
    • use the tip of the cap to break the seal and open the tube
    • wash the affected skin with soap and water and dry completely before applying
    •  apply 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
  • do not use if seal on tube is broken or is not visible
  • store at controlled room temperature 20-25°C (68-77°F)

Inactive ingredients

benzyl alcohol, cetyl alcohol, cetyl palmitate, isopropyl myristate, polysorbate 60, purified water, sodium hydroxide, sorbitan monostearate, stearyl alcohol.

Questions

call 1-800-452-0051

Novartis Consumer Health, Inc.

Parsippany, NJ 07054-0622 ©2008

Principal Display

LAMISIL  AT JOCK ITCH
terbinafine hydrochloride cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0067-3999
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TERBINAFINE HYDROCHLORIDE (TERBINAFINE) TERBINAFINE HYDROCHLORIDE10 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
BENZYL ALCOHOL 
CETYL ALCOHOL 
CETYL PALMITATE 
ISOPROPYL MYRISTATE 
POLYSORBATE 60 
WATER 
SODIUM HYDROXIDE 
SORBITAN MONOSTEARATE 
STEARYL ALCOHOL 
Packaging
#Item CodePackage Description
1NDC:0067-3999-421 TUBE (TUBE) in 1 CARTON
112 g in 1 TUBE
2NDC:0067-3999-151 TUBE (TUBE) in 1 CARTON
215 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA02098012/08/2006
Labeler - Novartis Consumer Health, Inc. (879821635)

Revised: 01/2010
 
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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