CLOTRIMAZOLE- clotrimazole cream 
Chain Drug Consortium, LLC

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Clotrimazole Vaginal Cream, USP

Drug Facts

Active ingredient

Clotrimazole, USP 1%

Purpose

Antifungal

Uses

Warnings

For external use only.

Do not use

on children under 2 years of age, unless directed by a doctor.

When using this product,

avoid contact with the eyes.

Stop use and ask a doctor if

  • irritation occurs
  • there is no improvement with 4 weeks (for athlete's foot and ringworm) or within 2 weeks (for jock itch)

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

Other information

Inactive ingredients

benzyl alcohol, cetostearyl alcohol, cetyl esters wax, 2-octyldodecanol, polysorbate 60, purified water, sodium phosphate monobasic, sorbitan monostearate

Questions or comments?

Call 1-877-753-3935 Monday-Friday 9AM-5PM EST

Principal display panel

COMPARE TO THE ACTIVE INGREDIENT IN LOTRIMIN® AF ATHLETE'S FOOT CREAM**

Clotrimazole Cream, USP 1%

ANTIFUNGAL CREAM

Proven Clinically Effective in the Treatment of the Most Athlete's Foot

*This product is not manufactured or distributed by Bayer HealthCare LLC., distributor of Lotrimin® AF Athlete's Foot Cream.

Distributed by:

Pharmacy Value Alliance, LLC

407 East Lancaster Avenue,

Wayne, PA 19087

Package label

Clotrimazole, USP 1%

PREMIER VALUE Antifungal Cream

CLOTRIMAZOLE 
clotrimazole cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68016-859
Route of AdministrationVAGINAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CLOTRIMAZOLE (UNII: G07GZ97H65) (CLOTRIMAZOLE - UNII:G07GZ97H65) CLOTRIMAZOLE10 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
BENZYL ALCOHOL (UNII: LKG8494WBH)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
CETYL ESTERS WAX (UNII: D072FFP9GU)  
OCTYLDODECANOL (UNII: 461N1O614Y)  
POLYSORBATE 60 (UNII: CAL22UVI4M)  
WATER (UNII: 059QF0KO0R)  
SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)  
SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68016-859-011 in 1 CARTON04/30/2021
128 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00504/30/2021
Labeler - Chain Drug Consortium, LLC (101668460)

Revised: 10/2023
Document Id: 3d8d9791-3fdb-4260-8053-7158099a2784
Set id: 9893c1a8-c834-4b1c-9325-204b5a573c71
Version: 4
Effective Time: 20231006
 
Chain Drug Consortium, LLC