CLOTRIMAZOLE ANTIFUNGAL- clotrimazole cream 
Army and Air Force Exchange Service

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Clotrimazole Cream 1%
ANTIFUNGAL

Drug Facts

Active ingredient

Clotrimazole 1%

Purpose

Antifungal

Uses

Warnings

For external use only

When using this product

  • do not get into the eyes

Stop use and ask a doctor if

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

Do not use

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

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

for athlete’s foot and ringworm

pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once every day. use every day for 4 weeks

for jock itch

use every day for 2 weeks. If condition lasts longer, contact a doctor.

Inactive ingredients

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

Questions?

1-800-432-8534 (select option #2) between 9 am and 4 pm EST, Monday–Friday.

Principal Display Panel

exchange select
*Compare to the active ingredient in Lotrimin® AF
CLOTRIMAZOLE CREAM 1%
ANTIFUNGAL
Cures Most Athlete’s Foot
Relieves Itching & Burning

Net Wt 1 oz (28 g)

exchange clotrimazole label1

CLOTRIMAZOLE ANTIFUNGAL 
clotrimazole cream
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:55301-350
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CLOTRIMAZOLE (UNII: G07GZ97H65) (CLOTRIMAZOLE - UNII:G07GZ97H65) CLOTRIMAZOLE 10 mg  in 1 g
Inactive Ingredients
Ingredient Name Strength
BENZYL ALCOHOL (UNII: LKG8494WBH)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
CETYL ESTERS WAX (UNII: D072FFP9GU)  
OCTYLDODECYL STEARATE (UNII: K6F16QGO28)  
POLYSORBATE 60 (UNII: CAL22UVI4M)  
WATER (UNII: 059QF0KO0R)  
SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)  
SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:55301-350-56 1 in 1 CARTON
1 28 g in 1 TUBE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH FINAL part333C 02/03/2006
Labeler - Army and Air Force Exchange Service (001695568)

Revised: 11/2013
Document Id: 7d2a8a16-bba5-425c-922b-5225a6ee6e69
Set id: 4de767b3-e9f5-45bf-b888-8c0615657dee
Version: 1
Effective Time: 20131113
 
Army and Air Force Exchange Service