Label: MCKESSON SKIN PROTECTANT- zinc oxide cream
- NDC Code(s): 68599-5312-1, 68599-5312-2, 68599-5312-6
- Packager: McKesson Medical-Surgical Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 11, 2024
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
Inactive ingredients
Purified Water, Cyclotetrasiloxane, Isopropyl Palmitate, Ethylhexyl Palmitate, Glycerin, Cyclopentasiloxane, Polyglyceryl-4 Isostearate,
Cetyl PEG/PPG-10/1 Dimethicone, Hexyl Laurate, Cetyl Dimethicone, Dimethicone, Tocopherol (Vitamin E), Zea Mays Oil, Retinyl Palmitate (Vitamin A), Cholecalciferol (Vitamin D3), Beeswax, Hydrogenated Castor Oil, Sodium Chloride, DMDM Hydantoin, Iodopropynyl Butylcarbamate - QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MCKESSON SKIN PROTECTANT
zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68599-5312 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 50 mg in 1 mL Inactive Ingredients Ingredient Name Strength CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB) DIMETHICONE (UNII: 92RU3N3Y1O) TOCOPHEROL (UNII: R0ZB2556P8) CORN OIL (UNII: 8470G57WFM) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) CHOLECALCIFEROL (UNII: 1C6V77QF41) YELLOW WAX (UNII: 2ZA36H0S2V) HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY) SODIUM CHLORIDE (UNII: 451W47IQ8X) DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) METHYLPARABEN (UNII: A2I8C7HI9T) WATER (UNII: 059QF0KO0R) CYCLOMETHICONE 4 (UNII: CZ227117JE) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) MINERAL OIL (UNII: T5L8T28FGP) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7) CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X) HEXYL LAURATE (UNII: 4CG9F9W01Q) ETHYLHEXYL PALMITATE (UNII: 2865993309) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68599-5312-1 24 in 1 CASE 10/25/2018 01/16/2019 1 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 2 NDC:68599-5312-2 24 in 1 CASE 10/25/2018 01/16/2019 2 207 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 3 NDC:68599-5312-6 24 in 1 CASE 10/25/2018 3 117 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 04/24/2014 Labeler - McKesson Medical-Surgical Inc. (023904428) Establishment Name Address ID/FEI Business Operations Central Solutions 007118524 manufacture(68599-5312)