CURIST  ANTIFUNGAL RELIEF- terbinafine hydrochloride cream 
Little Pharma, Inc.

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Curist
Antifungal Relief

Drug Facts

Active ingredient

Terbinafine hydrochloride 1%

Purpose

Antifungal

Uses

Warnings

For external use only

Do not use

  • on nails or scalp
  • in or near the mouth or the eyes
  • for vaginal yeast infections

When using this productdo not get into theeyes. If eye contact occurs, rinse thoroughly with water.

Stop use and ask a doctor iftoo 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 older:
    • 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 footwear 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 weekor as directed by a doctor.
      • on the bottom or sides of the foot:apply twice a day (morning and night) for 2 weeksor as directed by a doctor.
    • for jock itch and ringworm:apply once a day (morning ornight) for 1 weekor as directed by a doctor.
    • wash hands after each use
  • children under 12 years: ask a doctor
1 week between the toes
Figure
2 weeks on the bottom or sides of the foot
Figure

Other information

TAMPER EVIDENT: DO NOT USE IF THE SEAL ON THE TUBE IS PUNCTURED OR NOT VISIBLE.

Inactive ingredients

benzyl alcohol, cetyl alcohol, cetyl palmitate, isopropyl myristate, polysorbate 60, purified water, sodium hydroxide, sorbitan monostearate, stearyl alcohol

Questions?

Call 1-844-243-1241or email hi@curtisrelief.com

DISTRIBUTED BY:

Little Pharma, Inc.,

New York, NY 10023

Made in Canada

NDC: 72559-035-58

REV: 035-58-01

PRINCIPAL DISPLAY PANEL - 30 g Tube Carton

Curist

Antifungal Relief

Terbinafine Hydrochloride Cream 1%

Antifungal

NET WT. 1 OZ (30 g)

Carton Label

CURIST   ANTIFUNGAL RELIEF
terbinafine hydrochloride cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72559-035
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TERBINAFINE HYDROCHLORIDE (UNII: 012C11ZU6G) (TERBINAFINE - UNII:G7RIW8S0XP) TERBINAFINE1 g  in 100 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)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72559-035-581 in 1 CARTON12/10/2024
130 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07751112/10/2024
Labeler - Little Pharma, Inc. (074328189)

Revised: 6/2025
Document Id: 37a42ef8-419e-aad9-e063-6294a90a6a2a
Set id: 28f13725-48d1-8774-e063-6394a90a6704
Version: 3
Effective Time: 20250615
 
Little Pharma, Inc.