Lamisil AT Gel

Generic Name: terbinafine
Dosage Form: gel

Drug Facts

Active ingredient

Terbinafine1%

Purpose

Antifungal

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Uses

  • cures most athlete’s foot (tinea pedis) between the toes.

    Effectiveness on the bottom or sides of foot is unknown.

  • 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

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

Ask Doctor before use if you have

Ask a doctor or pharmacist

When using this product

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

Stop use and ask a doctor

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

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
    • for athlete’s footbetween the toes: apply once a day at bedtime for 1 week or as directed by a doctor. Wear well-fitting, ventilated shoes. Change shoes and socks at least once daily 
    • 1 week between the toes

    • for jock itch and ringworm: 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 or below 30°C (86°F)

Inactive ingredients

benzyl alcohol, butylated hydroxytoluene, carbomer 974 P, ethanol, isopropyl myristate, polysorbate 20, purified water, sodium hydroxide, sorbitan monolaurate

Questions

Questions? call 1-800-452-0051

 

Distributed by:

Novartis Consumer Health, Inc.

Parsippany, NJ 07054-0622

Principal Display Panel

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LAMISIL AT  ANTIFUNGAL
terbinafine gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0067-6239
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TERBINAFINE (TERBINAFINE) TERBINAFINE 10 mg  in 1 g
Inactive Ingredients
Ingredient Name Strength
ALCOHOL  
BENZYL ALCOHOL  
BUTYLATED HYDROXYTOLUENE  
ISOPROPYL MYRISTATE  
POLYSORBATE 20  
SODIUM HYDROXIDE  
SORBITAN MONOLAURATE  
WATER  
Packaging
# Item Code Package Description
1 NDC:0067-6239-42 1 TUBE (TUBE) in 1 CONTAINER
1 12 g in 1 TUBE
2 NDC:0067-6239-21 1 TUBE (TUBE) in 1 CONTAINER
2 6 g in 1 TUBE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA021958 01/01/2010
Labeler - Novartis Consumer Health, Inc. (879821635)
Revised: 01/2010
 
Novartis Consumer Health, Inc.



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