Lamisil AT description, usages, side effects, indications, overdosage, supplying and lots more!

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Lamisil AT

Novartis Consumer Health, Inc.
Taro Pharmaceuticals U.S.A., Inc.

Lamisil AT for Jock Itch


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Terbinafine hydrochloride 1%

Purpose

Antifungal

Lamisil AT Uses

  • cures most jock itch (tinea cruris)
  • 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 eyes
  • for vaginal yeast infections

When using this product do not get into the eyes. If eye contact occurs, rinse 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.

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

Lamisil AT 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?

call 1-800-452-0051

Distributed by: Novartis Consumer Health, Inc.
Parsippany, NJ 07054-0622

PRINCIPAL DISPLAY PANEL - 12 g Tube Carton

TERBINAFINE HYDROCHLORIDE CREAM 1% - ANTIFUNGAL

LAMISIL AT®

CREAM for
JOCK ITCH

Relieves itching and burning

Net Wt. 12 g (.42 oz)

Lamisil AT

Lamisil AT

Terbinafine Hydrochloride CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0067-8114
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
TERBINAFINE HYDROCHLORIDE Terbinafine 1 g

Inactive Ingredients

Ingredient Name Strength
BENZYL ALCOHOL
CETYL ALCOHOL
cetyl palmitate
ISOPROPYL MYRISTATE
POLYSORBATE 60
water
SODIUM HYDROXIDE
SORBITAN MONOSTEARATE
stearyl alcohol

Product Characteristics

Color
WHITE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 12 in 1 TUBE
2 NDC:0067-8114-12 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA077511 2007-07-02


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Be sure to consult your doctor before taking any medication!
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