POTASSIUM CHLORIDE- potassium chloride solution 
Westminster Pharmaceuticals, LLC

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.

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Potassium Chloride Oral Solution, USP 10 %

INSTRUCTIONS FOR USE SECTION

To minimize gastrointestinal irritation, patients must follow direction regarding dilution. Each tablespoon (15mL) should be diluted with three (3) fluid ounce or more of water or other liquid.

DOSAGE FORM AND STRENGTH

Adult Dosage: one (1) tablespoon (15mL) twice daily (after morning or evening meals) supplies 40mEq of potassium.

For treatment of patient with hypokalemia, with or without metabolic alkalosis, in digitalis intoxication.

PACKAGE LABEL PRINCIPAL DISPLAY PANEL

Potassium Chloride Solution

POTASSIUM CHLORIDE 
potassium chloride solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:69367-101
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
potassium chloride (UNII: 660YQ98I10) (potassium cation - UNII:295O53K152) potassium cation1.3 meq  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Methylparaben (UNII: A2I8C7HI9T)  
sodium citrate (UNII: 1Q73Q2JULR)  
D&C Red No. 33 (UNII: 9DBA0SBB0L)  
propylene glycol (UNII: 6DC9Q167V3)  
water (UNII: 059QF0KO0R)  
saccharin sodium (UNII: SB8ZUX40TY)  
propylparaben (UNII: Z8IX2SC1OH)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
glycerin (UNII: PDC6A3C0OX)  
Product Characteristics
ColorpinkScore    
ShapeSize
FlavorCHERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69367-101-16473 mL in 1 BOTTLE; Type 0: Not a Combination Product01/22/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other01/22/201510/02/2015
Labeler - Westminster Pharmaceuticals, LLC (079516651)

Revised: 10/2015
Document Id: 2124cba8-c932-4ffe-e054-00144ff8d46c
Set id: 0b35cd59-0caa-4ba5-e054-00144ff8d46c
Version: 5
Effective Time: 20151002
 
Westminster Pharmaceuticals, LLC