Label: DERMAMED- skin protectant ointment
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Contains inactivated NDC Code(s)
NDC Code(s): 61924-214-04 - Packager: DermaRite Industries, LLC
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated January 17, 2020
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INGREDIENTS AND APPEARANCE
DERMAMED
skin protectant ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61924-214 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0) ALUMINUM HYDROXIDE 2 g in 100 g Inactive Ingredients Ingredient Name Strength CHOLECALCIFEROL (UNII: 1C6V77QF41) LANOLIN (UNII: 7EV65EAW6H) LANOLIN ALCOHOLS (UNII: 884C3FA9HE) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) PROPYLENE GLYCOL 1-(2-METHYLBUTYRATE) (UNII: 9Q5W5G6461) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) DMDM HYDANTOIN (UNII: BYR0546TOW) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) CORN OIL (UNII: 8470G57WFM) METHYLPARABEN (UNII: A2I8C7HI9T) SODIUM CHLORIDE (UNII: 451W47IQ8X) ZINC CHLORIDE (UNII: 86Q357L16B) PROPYLPARABEN (UNII: Z8IX2SC1OH) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) PETROLATUM (UNII: 4T6H12BN9U) CALCIUM CARBONATE (UNII: H0G9379FGK) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61924-214-04 106 g in 1 TUBE; Type 0: Not a Combination Product 10/18/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 10/18/2016 Labeler - DermaRite Industries, LLC (883925562) Registrant - DermaRite Industries, LLC (883925562) Establishment Name Address ID/FEI Business Operations DermaRite Industries, LLC 883925562 manufacture(61924-214)