Label: DERMADROX- aluminum hydroxide ointment
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Contains inactivated NDC Code(s)
NDC Code(s): 54162-221-04 - Packager: GERITREX LLC
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated October 20, 2016
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INGREDIENTS AND APPEARANCE
DERMADROX
aluminum hydroxide ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54162-221 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0) ALUMINUM HYDROXIDE 1.356 g in 113 g Inactive Ingredients Ingredient Name Strength CALCIUM CARBONATE (UNII: H0G9379FGK) CITRIC ACID ACETATE (UNII: DSO12WL7AU) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) LANOLIN (UNII: 7EV65EAW6H) LANOLIN ALCOHOLS (UNII: 884C3FA9HE) MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) MINERAL OIL (UNII: T5L8T28FGP) PETROLATUM (UNII: 4T6H12BN9U) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) VITAMIN A (UNII: 81G40H8B0T) VITAMIN D (UNII: 9VU1KI44GP) ZINC CHLORIDE (UNII: 86Q357L16B) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54162-221-04 113 g in 1 JAR; Type 0: Not a Combination Product 07/31/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 10/15/2013 Labeler - GERITREX LLC (112796248) Registrant - GERITREX LLC (112796248) Establishment Name Address ID/FEI Business Operations GERITREX LLC 112796248 manufacture(54162-221)