JOCK ITCH- clotrimazole cream
Walgreen Company

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, USP

Drug Facts

Active ingredient

Clotrimazole, USP 1%

Purpose

Antifungal

Uses

• cures most jock itch • relieves itching, burning, scaling, discomfort, and chafing associated with jock itch

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 within 2 weeks

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• wash the affected area and dry thoroughly
• apply a thin layer of the product over affected area twice daily (morning and night), or as directed by a doctor
• supervise children in the use of this product
• use daily for 2 weeks
• if condition lasts longer, ask a doctor
• this product is not effective on the scalp or nails

Other information

• Store between 2°-30°C (36°-86°F).
• Before using any medication, read all label directions • Keep carton, it contains important information

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 between 9 am and 4 pm EST, Monday – Friday.

Principal Display Panel

Walgreens
NDC 0363-3510-34

Jock Itch Cream
Clotrimazole Cream, USP 1%
Antifungal Cream

Proven clinically effective in the treatment of most jock itch
Relieves itching, burning, scaling & chafing

Compare to Lotrimin® AF active ingredient#

Cures most jock itch.

NET WT 0.5 OZ (14 g)

JOCK ITCH
clotrimazole cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0363-3510
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CLOTRIMAZOLE (UNII: G07GZ97H65) (CLOTRIMAZOLE - UNII:G07GZ97H65)	CLOTRIMAZOLE	1 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
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, ANHYDROUS (UNII: KH7I04HPUU)
SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0363-3510-34	1 in 1 CARTON	06/15/2014	11/01/2016
1		14 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC MONOGRAPH FINAL	part333C	06/15/2014	11/01/2016

Labeler - Walgreen Company (008965063)

Registrant - Teva Pharmaceuticals USA, Inc. (001627975)

Revised: 5/2019

Document Id: 57630df3-cf7c-4146-9ee9-1e93ce2a7cbc

Set id: 29fbce15-64fa-4d9e-8c1b-4d3ddb329e43

Version: 7

Effective Time: 20190529

Walgreen Company