Label: LAMISIL AT CREAM- terbinafine hydrochloride cream
- NDC Code(s): 84485-4030-1
- Packager: Karo Healthcare Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: New Drug Application
Drug Label Information
Updated October 2, 2025
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- Official Label (Printer Friendly)
- Active Ingredient
- Uses
- Warnings
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Directions
- •
- adults and children 12 years and over:
- o
- use the tip of the cap to break the seal and open the tube
- o
- wash the affected skin with soap and water and dry completely before applying
- o
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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
- o
- for jock itch and ringworm: apply once a day (morning or night) for 1 week or as directed by a doctor
- o
- wash hands after each use
- •
- children under 12 years: ask a doctor
- Other Information
- Inactive Ingredients
- Questions or comments?
-
PACKAGE LABEL.PRINCIPAL DISPLAY
LAMISILAT
CREAM
TERBINAFINE HYDROCHLORIDE
CREAM 1% - ANTIFUNGAL
ALL-IN-ONEATHLETE'S FOOT, JOCK ITCH, RINGWORM
►Clinically proven to cure most athlete’s foot, jock itch and ringworm
► Effective relief of itching, burning, cracking and scaling
► FULL PRESCRIPTION STRENGTH
NET WT 12 g (0.42 oz)
RECYCLABLE CARTON
1-888-544-1880
Distributed By:
Karo Healthcare Inc.
Morristown, NJ 07960 USA
Trademarks owned or
licensed By Karo Healthcare
©2025 Karo Healthcare
2005210_1 Made in Canada
LAMISILAT CREAM
TERBINAFINE HYDROCHLORIDE CREAM 1% - ANTIFUNGAL
FOR ATHLETE'S FOOT, JOCK ITCH, RINGWORM
NET WT
12g (0.42 oz)
2005211_1 -
INGREDIENTS AND APPEARANCE
LAMISIL AT CREAM
terbinafine hydrochloride creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84485-4030 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:84485-4030-1 1 in 1 CARTON 10/09/2025 1 12 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 10/09/2025 Labeler - Karo Healthcare Inc. (119195452)


