Label: ATHLETES FOOT- clotrimazole cream
- NDC Code(s): 0363-1857-58, 0363-1857-64
- Packager: Walgreen Company
- Category: HUMAN OTC DRUG LABEL
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 May 30, 2019
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- Active ingredient
- Purpose
- Uses
- Warnings
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Directions
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- wash the affected area and dry thoroughly
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- apply a thin layer over affected area twice daily (morning and night)
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- supervise children in the use of this product
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- for athlete’s foot pay special attention to the spaces between the toes, wear well-fitting ventilated shoes and change shoes and socks at least once daily
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- for athlete’s foot and ringworm, use daily for 4 weeks; for jock itch, use daily for 2 weeks
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- if condition persists longer, consult a doctor
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- this product is not effective on the scalp or nails
- Other information
- Inactive ingredients
- Questions or comments?
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INGREDIENTS AND APPEARANCE
ATHLETES FOOT
clotrimazole creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-1857 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CLOTRIMAZOLE (UNII: G07GZ97H65) (CLOTRIMAZOLE - UNII:G07GZ97H65) CLOTRIMAZOLE 1 g in 100 g Inactive Ingredients Ingredient Name Strength BENZYL ALCOHOL (UNII: LKG8494WBH) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETYL ESTERS WAX (UNII: D072FFP9GU) OCTYLDODECANOL (UNII: 461N1O614Y) POLYSORBATE 60 (UNII: CAL22UVI4M) WATER (UNII: 059QF0KO0R) SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-1857-64 1 in 1 CARTON 09/29/2017 1 28 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:0363-1857-58 1 in 1 CARTON 03/15/2018 2 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 final part333C 09/29/2017 Labeler - Walgreen Company (008965063)