K-Phos No. 2

Name: K-Phos No. 2

How should I take this medicine?

Follow all directions on your prescription label. Do not take this medicine in larger or smaller amounts or for longer than recommended.

Take this medicine with a full glass of water.

Potassium phosphate and sodium phosphate works best if you take it with meals and at bedtime.

While using this medicine, you may need frequent blood or urine tests.

The powder form must be mixed with water before you take it. Mix 1 packet of the powder with about 1/3 cup (2.5 ounces) of water and stir until completely dissolved. Swallow the mixture right away after mixing. Do not save for later use.

The tablet form may need to be dissolved in water, or swallowed whole. Carefully follow any dosing instructions provided with your medicine.

If you have a history of kidney stones, it is possible that you will pass old stones after starting treatment with potassium phosphate and sodium phosphate.

Store at room temperature away from moisture, heat, and light. Keep the bottle tightly closed when not in use.

K-PHOS® No. 2 Urinary Acidifier

Rx ONLY

Indicatons and usage

K-PHOS® No. 2 is a highly effective urinary acidifier for use in patients with elevated urinary pH. This product helps keep calcium soluble and reduces odor and rash caused by ammoniacal urine. Also, by acidifying the urine, it increases the antibacterial activity of methenamine mandelate and methenamine hippurate.

Contraindications

This product is contraindicated in patients with infected phosphate stones, in patients with severely impaired renal function (less than 30% of normal) and in the presence of hyperphosphatemia.

PRINCIPAL DISPLAY PANEL - 250 mg Tablet Bottle Label

NDC 0486-1134-01

K-PHOS® No. 2
URINARY ACIDIFIER

Each tablet supplies
250 mg of phosphorus

Rx ONLY

100 TABLETS

Beach

K-PHOS   NO. 2
potassium phosphate, monobasic and sodium phosphate, monobasic, anhydrous tablet, coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:0486-1134
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Potassium Phosphate, Monobasic (Phosphate Ion and Potassium Cation) Potassium Phosphate, Monobasic 305 mg
Sodium Phosphate, Monobasic, Anhydrous (Phosphate Ion and Sodium Cation) Sodium Phosphate, Monobasic, Anhydrous 700 mg
Inactive Ingredients
Ingredient Name Strength
Lactose  
Magnesium Stearate  
Cellulose, Microcrystalline  
Povidones  
Water O-18  
Sodium Starch Glycolate Type A Potato  
Stearic Acid  
Talc  
FD&C Blue No. 2  
FD&C Red No. 40  
FD&C Yellow No. 6  
Hypromelloses  
Polyethylene Glycols  
Polydextrose  
Titanium Dioxide  
Triacetin  
Product Characteristics
Color BROWN Score no score
Shape OVAL Size 19mm
Flavor Imprint Code BEACH;11;34
Contains     
Packaging
# Item Code Package Description
1 NDC:0486-1134-01 100 TABLET, COATED in 1 BOTTLE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
UNAPPROVED DRUG OTHER 05/09/1978
Labeler - Beach Products, Inc. (032763633)
Establishment
Name Address ID/FEI Operations
Gillette Manufacturing 160356114 MANUFACTURE(0486-1134)
Revised: 10/2014   Beach Products, Inc.
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