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Lamisil AT Jock Itch

Package insert / prescribing information
Generic name: terbinafine hydrochloride
Dosage form: cream
Drug class: Topical antifungals

Medically reviewed by Drugs.com. Last updated on Jun 1, 2021.

Active ingredient

Terbinafine hydrochloride 1%

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

on nails or scalp
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 or comments?

call 1-800-330-9876

Distributed by: GSK Consumer Healthcare, Warren, NJ 07059

Trademarks owned or licensed by GSK.

©2019 GSK or licensor.

13510 (Front Carton)

Principal Display Panel

NDC 0067-3999-42

LAMISIL AT CREAM

gsk

TERBINAFINE HYDROCHLORIDE CREAM 1% - ANTIFUNGAL

FOR JOCK ITCH

NET WT 12 g (0.42 oz)

13510 (Front Carton)

LAMISIL AT JOCK ITCH
terbinafine hydrochloride cream
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0067-3999
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TERBINAFINE HYDROCHLORIDE (TERBINAFINE) TERBINAFINE HYDROCHLORIDE 10 mg in 1 g
Inactive Ingredients
Ingredient Name Strength
BENZYL ALCOHOL
CETYL ALCOHOL
CETYL PALMITATE
ISOPROPYL MYRISTATE
POLYSORBATE 60
WATER
SODIUM HYDROXIDE
SORBITAN MONOSTEARATE
STEARYL ALCOHOL
Packaging
# Item Code Package Description
1 NDC:0067-3999-42 1 TUBE in 1 CARTON
1 12 g in 1 TUBE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA020980 12/08/2006
Labeler - GlaxoSmithKline Consumer Healthcare Holdings (US) LLC (079944263)
GlaxoSmithKline Consumer Healthcare Holdings (US) LLC

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