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Lamisil AT Jock Itch: Package Insert / Prescribing Info

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

Medically reviewed by Drugs.com. Last updated on Feb 28, 2024.

Active ingredient

Terbinafine hydrochloride 1%

Purpose

Antifungal

Indications and Usage for Lamisil AT Jock Itch

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.

Lamisil AT Jock Itch Dosage and Administration

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

Storage and Handling

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)

13510 Lamisil AT JI 12g (0.42 oz)
LAMISIL AT JOCK ITCH
terbinafine hydrochloride cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0067-3999
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TERBINAFINE HYDROCHLORIDE (UNII: 012C11ZU6G) (TERBINAFINE - UNII:G7RIW8S0XP) TERBINAFINE HYDROCHLORIDE10 mg in 1 g
Inactive Ingredients
Ingredient NameStrength
BENZYL ALCOHOL (UNII: LKG8494WBH)
CETYL ALCOHOL (UNII: 936JST6JCN)
CETYL PALMITATE (UNII: 5ZA2S6B08X)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
POLYSORBATE 60 (UNII: CAL22UVI4M)
WATER (UNII: 059QF0KO0R)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0067-3999-421 in 1 CARTON12/08/2006
112 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA02098012/08/2006
Labeler - GlaxoSmithKline Consumer Healthcare Holdings (US) LLC (079944263)

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