Label: LUMICAIN- aluminium chloride hexahydrate solution
- NDC Code(s): 10733-412-60
- Packager: Medical Products Laboratories, Inc.
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated December 23, 2020
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INGREDIENTS AND APPEARANCE
LUMICAIN
aluminium chloride hexahydrate solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:10733-412 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM CHLORIDE (UNII: 3CYT62D3GA) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM CHLORIDE 250 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10733-412-60 67 g in 1 BOTTLE; Type 0: Not a Combination Product 09/29/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/29/2010 Labeler - Medical Products Laboratories, Inc. (002290302) Registrant - Medical Products Laboratories, Inc. (002290302) Establishment Name Address ID/FEI Business Operations Medical Products Laboratories, Inc. 002290302 analysis(10733-412) , manufacture(10733-412) , label(10733-412) , pack(10733-412)