Label: MENTHOLATUM HEEL REVIVAL CREAM cream
- NDC Code(s): 10742-0020-1
- Packager: The Mentholatum Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated September 9, 2024
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- Active ingredient
- Purpose
- Uses
- Warnings
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Directions
- clean 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
- for athlete’s foot: pay special attention to the areas between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily
- for athlete's foot, use daily for 4 weeks. If condition persists longer, consult a doctor
- this product is not effective on the scalp or nails
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Inactive ingredients
water, caprylic/capric triglyceride, urea, cetyl alcohol, glycerin, glycine, hexadecane, tridecyl stearate, ethoxydiglycol, ceteth-23, polyacrylate crosspolymer-6, diethyl sebacate, dimethicone, hydroxyethylcellulose, lactic acid, phenoxyethanol, propylene glycol caprylate, simmondsia chinensis (jojoba) seed oil, sodium dilauramidoglutamide lysine, sorbitan stearate, squalane, zinc oxide
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INGREDIENTS AND APPEARANCE
MENTHOLATUM HEEL REVIVAL CREAM
mentholatum heel revival cream creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10742-0020 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV) TOLNAFTATE 10 mg in 1 g Inactive Ingredients Ingredient Name Strength ZINC OXIDE (UNII: SOI2LOH54Z) GLYCERIN (UNII: PDC6A3C0OX) ETHOXYDIGLYCOL (UNII: A1A1I8X02B) DIPROPYLENE GLYCOL CAPRYLATE (UNII: CJ981S4H3T) CETETH-23 (UNII: 495CTZ441V) SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL (UNII: 724GKU717M) WATER (UNII: 059QF0KO0R) CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U) DIETHYL SEBACATE (UNII: I41B9FJK6V) SORBITAN STEARATE (UNII: NVZ4I0H58X) PHENOXYETHANOL (UNII: HIE492ZZ3T) HEXADECANE (UNII: F8Z00SHP6Q) POLYACRYLATE CROSSPOLYMER-6 (UNII: Q7UI015FF9) CETYL ALCOHOL (UNII: 936JST6JCN) LACTIC ACID (UNII: 33X04XA5AT) DIMETHICONE (UNII: 92RU3N3Y1O) UREA (UNII: 8W8T17847W) HYDROXYETHYLCELLULOSE (UNII: T4V6TWG28D) SQUALANE (UNII: GW89575KF9) GLYCINE (UNII: TE7660XO1C) SODIUM DILAURAMIDOGLUTAMIDE LYSINE (UNII: MNJ7VPT2R5) TRIDECYL STEARATE (UNII: A8OE252M6L) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10742-0020-1 1 in 1 CARTON 09/30/2024 1 28 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 09/12/2024 Labeler - The Mentholatum Company (002105757) Registrant - The Mentholatum Company (002105757) Establishment Name Address ID/FEI Business Operations The Mentholatum Company 002105757 manufacture(10742-0020)