Label: ANTIFUNGAL 1% CLOTRIMAZOLE CREAM cream
- NDC Code(s): 70856-3585-1
- Packager: Defense Soap LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 16, 2024
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
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Inactive Ingredients
Inactive ingredients: Allantoin, Avena Sativa (Oat) Kemel Flour, Butyrospermum Parkii (Shea) Butter,
Calophyllum Tacamahaca Seed Oil, Carthamus Tinctorius (Safflower) Seed Oil, Cellulose Gum, Cetearyl Alcohol,
Citric Acid, Ethylhexyl Palmitate, Glycerin, Glyceryl Stearate. Melia Azadirachta Seed Oil, Microcrystalline
Cellulose, PEG-100 Stearate, Phenoxyethanol, Propylene Glycol, Sodium Gluconate, Sodium Polyacrylate Starch,
Urea, Water, Xanthan Gum
- Active Ingredient
- Purpose
- Warnings
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Directions
Directions Wash and diy affected area thoroughly. Apply a thin layer over affected area twice daily
(moming and night). Supervise children in the use of this product. 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. For athlete’s foot and ringworm. use daily for 4 weeks. For jock itch, use daily for 2 weeks. If
condition persists longer, ask a doctor. This product is not effective on the scalp or nails
- Uses
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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 eyes.
Stop use and ask a doctor if irritation occurrs or if there is no improvement within 2 weeks for jock itch or within 4 weeks for athlete's foot and ringworm.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. - Artwork
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INGREDIENTS AND APPEARANCE
ANTIFUNGAL 1% CLOTRIMAZOLE CREAM
antifungal 1% clotrimazole cream creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70856-3585 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 mL Inactive Ingredients Ingredient Name Strength UREA (UNII: 8W8T17847W) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) CALOPHYLLUM TACAMAHACA SEED OIL (UNII: 05G85L61OE) ETHYLHEXYL PALMITATE (UNII: 2865993309) PHENOXYETHANOL (UNII: HIE492ZZ3T) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) AZADIRACHTA INDICA SEED OIL (UNII: 4DKJ9B3K2T) SHEA BUTTER (UNII: K49155WL9Y) SODIUM GLUCONATE (UNII: R6Q3791S76) XANTHAN GUM (UNII: TTV12P4NEE) OATMEAL (UNII: 8PI54V663Y) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) SAFFLOWER OIL (UNII: 65UEH262IS) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) PEG-100 STEARATE (UNII: YD01N1999R) SODIUM POLYACRYLATE STARCH (25 MICROMETER PARTICLE) (UNII: KXY4EH7RJV) ALLANTOIN (UNII: 344S277G0Z) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) Product Characteristics Color white (Opaque Cream) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70856-3585-1 1 in 1 CARTON 10/01/2024 1 29.5 mL 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 10/01/2024 Labeler - Defense Soap LLC (780587353)
