Label: JOCK ITCH CLOTRIMAZOLE ANTIFUNGAL- clotrimazole cream
- NDC Code(s): 49035-837-05
- Packager: Walmart
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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.
Drug Label Information
Updated January 19, 2022
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Warnings
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Directions
- wash affected area and dry thoroughly
- apply a thin layer over affected area twice daily (morning and night)
- supervise children in use of this product
- for athlete's foot, pay special attention to spaces between the toes, wear well-fitting, ventilated shoes and change shoes and socks at least once daily
- for athlete's foot and ringworm, use daily for 4 weeks; for jock itch, use daily for 2 weeks
- if condition persists longer, consult a doctor
- this product is not effective on scalp or nails
- Other information
- Inactive ingredient
- Questions or comments?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 14.2 g Tube Carton
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INGREDIENTS AND APPEARANCE
JOCK ITCH CLOTRIMAZOLE ANTIFUNGAL
clotrimazole creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-837 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Clotrimazole (UNII: G07GZ97H65) (Clotrimazole - UNII:G07GZ97H65) Clotrimazole 0.01 g in 1 g Inactive Ingredients Ingredient Name Strength Aloe Vera Leaf (UNII: ZY81Z83H0X) Benzyl Alcohol (UNII: LKG8494WBH) Cetostearyl Alcohol (UNII: 2DMT128M1S) Cetyl Esters Wax (UNII: D072FFP9GU) Octyldodecanol (UNII: 461N1O614Y) Polysorbate 60 (UNII: CAL22UVI4M) Sorbitan Monostearate (UNII: NVZ4I0H58X) .Alpha.-Tocopherol Acetate, Dl- (UNII: WR1WPI7EW8) Water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49035-837-05 1 in 1 CARTON 08/31/1993 1 14.2 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 FINAL part333C 08/31/1993 Labeler - Walmart (051957769) Establishment Name Address ID/FEI Business Operations Natureplex, LLC 062808196 MANUFACTURE(49035-837)