K Phos Original

POTASSIUM PHOSPHATE, MONOBASIC ORAL HUMAN PRESCRIPTION DRUG

K Phos Original is an FDA drug label for the active ingredient POTASSIUM PHOSPHATE, MONOBASIC manufactured by Beach Products, Inc. administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20230223.

Generic name
POTASSIUM PHOSPHATE, MONOBASIC
Manufacturer
Beach Products, Inc.
Product type
HUMAN PRESCRIPTION DRUG
Route
ORAL
Dosage form
N/A
NDC
0486-1111
Application
N/A
Label effective
20230223

About this product

K Phos Original is an FDA-registered drug product whose active ingredient is POTASSIUM PHOSPHATE, MONOBASIC. It is labelled by Beach Products, Inc. taken by oral and marketed as a human prescription drug product. Identifiers on file: NDC 0486-1111, label effective 20230223. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

What it is used for

Across FDA labelling, products containing POTASSIUM PHOSPHATE, MONOBASIC are most often described in connection with: elevated urinary, k-phos original, helps keep, calcium soluble, reduces odor, rash caused, ammoniacal urine, antibacterial activity. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Indications & Usage

INDICATONS AND USAGE For use in patients with elevated urinary pH. K-PHOS® ORIGINAL 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.

Dosage & Administration

DOSAGE AND ADMINISTRATION Two tablets dissolved in 6-8 oz. of water 4 times daily with meals and at bedtime. For best results, let the tablets soak in water for 2 to 5 minutes, or more if necessary, and stir. If any tablet particles remain undissolved, they may be crushed and stirred vigorously to speed dissolution.

Contraindications

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 and hyperkalemia.

Adverse Reactions

ADVERSE REACTIONS Gastrointestinal upset (diarrhea, nausea, stomach pain, and vomiting) may occur with the use of potassium phosphate. Also, bone and joint pain (possible phosphate-induced osteomalacia) could occur. The following adverse effects may be observed with potassium administration: irregular heartbeat; dizziness; mental confusion; weakness or heaviness of legs; unusual tiredness; muscle cramps; numbness, tingling, pain, or weakness in hands or feet; numbness or tingling around lips; shortness of breath or troubled breathing.

Frequently asked questions

What is K Phos Original used for?
INDICATONS AND USAGE For use in patients with elevated urinary pH. K-PHOS® ORIGINAL 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.

Who makes K Phos Original?
Beach Products, Inc. is the labeler of record for K Phos Original.

What form does K Phos Original come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is K Phos Original prescription or over-the-counter?
The FDA label for this product is recorded as human prescription drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Has K Phos Original been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.