JOCK-EZE- clotrimazole cream

JOCK-EZE by

Drug Labeling and Warnings

JOCK-EZE by is a Otc medication manufactured, distributed, or labeled by Bentlin Products LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Clotrimazole 1 %

Purpose

Antifungal Cream

Uses

Cures most jock itch (tinea cruris). Relieves the itching, irritation, redness, scaling and discomfort which can accompany these conditions.

Warnings

• Keep this and all drugs out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

• Clean the affected area and dry thoroughly.
• Apply a thin layer of this product over affected area twice daily (morning and night), or as directed by a doctor.
• Supervise children in the use of this product.
• For jock itch, use daily for 2 weeks.
• If conditions persist longer, consult a doctor.
• This product is not effective on the scalp or nails.

Other information

• Store at controlled room temperature 68°-77°F (20°-25°C).
• Close cap tightly after use.

Inactive ingredients

Aloe Barbadensis Leaf Juice, Benzyl Alcohol, Cetearyl Alcohol, Cetyl Esters, Octyldodecanol, Polysorbate 60, Sorbitan Monostearate, Tocopheryl Acetate, Purified Water.

Questions?

888-445-1610

Principal Display Panel – 0.5oz Tube

JOCK-EZE                NDC: 47832-071-14

Flare Control Cream for Jock Itch 

Clotrimazole 1% Antifungal Cream 

NET WT. 0.5oz (14g)

Principal Display Panel – 0.5oz Carton

NDC: 47382-071-14

JOCK-EZE

Flare Control Cream for Jock Itch 

Clotrimazole 1% Antifungal Cream 

NET WT. 0.5oz (14g)

INGREDIENTS AND APPEARANCE

JOCK-EZE 
clotrimazole cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47832-071
Route of Administration	TOPICAL

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
WATER (UNII: 059QF0KO0R)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
POLYSORBATE 60 (UNII: CAL22UVI4M)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
OCTYLDODECANOL (UNII: 461N1O614Y)
CETYL PALMITATE (UNII: 5ZA2S6B08X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47832-071-14	1 in 1 CARTON	01/21/2020
1		14 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	01/21/2020

Labeler - Bentlin Products LLC (832615426)