Label: LAMISIL AT CREAM- terbinafine hydrochloride cream
- NDC Code(s): 84485-3748-3
- Packager: Karo Healthcare Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated January 9, 2025
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- Active Ingredient
- Uses
- Warnings
-
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 foot wear well-fitting, ventilated shoes. Change shoes and socks at least once daily.
- between the toes only: apply twice a day (morning and night) for 1 week or as directed by a doctor
- on the bottom or sides of the foot: apply twice a day (morning and night) for 2 weeks or as directed by a doctor
- 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
- adults and children 12 years and over:
- Other Information
- Inactive Ingredients
- Questions or comments?
-
PACKAGE LABEL.PRINCIPAL DISPLAY
LAMISILAT
CREAM
TERBINAFINE HYDROCHLORIDE
CREAM 1% - ANTIFUNGAL
FOR ATHLETE'S FOOT
►RELIEVES ITCHING
► CLINICALLY PROVEN TO CURE MOST ATHLETE’S FOOT BETWEEN THE TOES
► FULL PRESCRIPTION STRENGTH
NET WT 30 g (1 oz)
RECYCLABLE CARTON
Distributed by: Karo Healthcare Inc.
Morristown, NJ 07960 USA
Made in Canada
Trademarks owned or licensed
by Karo Healthcare
©2024 Karo Healthcare
or licensor.
1-888-544-1880
NDC
84485-3748-3
2004439_1

2003665_1

LAMISILAT CREAM
TERBINAFINE HYDROCHLORIDE CREAM 1% - ANTIFUNGAL
FOR ATHLETE'S FOOT
NET WT
30g (1 oz)
2004440_1
-
INGREDIENTS AND APPEARANCE
LAMISIL AT CREAM
terbinafine hydrochloride creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84485-3748 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TERBINAFINE HYDROCHLORIDE (UNII: 012C11ZU6G) (TERBINAFINE - UNII:G7RIW8S0XP) TERBINAFINE HYDROCHLORIDE 1 g in 100 g Inactive Ingredients Ingredient Name Strength CETYL ALCOHOL (UNII: 936JST6JCN) POLYSORBATE 60 (UNII: CAL22UVI4M) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) BENZYL ALCOHOL (UNII: LKG8494WBH) CETYL PALMITATE (UNII: 5ZA2S6B08X) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) WATER (UNII: 059QF0KO0R) SODIUM HYDROXIDE (UNII: 55X04QC32I) SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84485-3748-3 1 in 1 CARTON 11/01/2024 1 30 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA020980 11/01/2024 Labeler - Karo Healthcare Inc. (119195452)
