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
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Updated December 23, 2020
If you are a consumer or patient please visit this version.
- DOSAGE & ADMINISTRATION
- WARNINGS AND PRECAUTIONS
- PRINCIPAL DISPLAY PANEL
INGREDIENTS AND APPEARANCE
aluminium chloride hexahydrate solution
Product 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)