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Lamisil AT Spray Prescribing Information

Package insert / product label
Generic name: terbinafine hydrochloride
Dosage form: spray
Drug class: Topical antifungals

Medically reviewed by Drugs.com. Last updated on Mar 25, 2024.

Active ingredient

Terbinafine hydrochloride

Purpose

Antifungal

Indications and Usage for Lamisil AT Spray

  • 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 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.

Lamisil AT Spray Dosage and Administration

  • adults and children 12 years and over
    • wash the affected skin with soap and water and dry completely before applying
    • for athlete’s foot between the toes spray twice a day (morning and night) for 1 week or as directed by a doctor. Wear well-fitting, ventilated shoes. Change shoes and socks at least once daily.
    • for jock itch and ringworm 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
fott image

Storage and Handling

store at 8° - 25° C (46° - 77° F)

Questions? call 1-800-452-0051

Distributed by: Novartis Consumer Health, Inc.

Parsippany, NJ 07054-0622

Inactive ingredients

cetomacrogol, ethanol, propylene glycol, purified water

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Carton image
LAMISIL AT
terbinafine hydrochloride spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0067-4001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TERBINAFINE HYDROCHLORIDE (UNII: 012C11ZU6G) (TERBINAFINE - UNII:G7RIW8S0XP) TERBINAFINE HYDROCHLORIDE1 mL in 100 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)
CETETH-20 (UNII: I835H2IHHX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0067-4001-0130 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA02112407/23/200906/15/2012
Labeler - Novartis Consumer Health, Inc. (879821635)

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