Prescription drug · UNAPPROVED DRUG OTHER
K Phos Original (Potassium phosphate, monobasic) NDC 0486-1111
Potassium phosphate, Monobasic 500 mg/1 · Tablet, Soluble · Oral · Beach Products, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 0486-1111-01 | 0048611110100486111101 | 100 TABLET, SOLUBLE in 1 BOTTLE (0486-1111-01)Marketed from Mar 29, 1977 | |
| 0486-1111-05 | 0048611110500486111105 | 500 TABLET, SOLUBLE in 1 BOTTLE (0486-1111-05)Marketed from Mar 29, 1977 |
How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- K Phos OriginalSuffix: Original
- Generic name (nonproprietary)
- potassium phosphate, monobasic
- Active ingredients
- Potassium phosphate, Monobasic — 500 mg/1
- Dosage form
- Tablet, Soluble
- Route
- Oral
- Labeler
- Beach Products, Inc.NDC labeler code 0486
- Product type
- Prescription drug
- Marketing category
- Unapproved drug (other)
- Marketing start
- Listing expires
- Identifiers
- Product ID 0486-1111_5cdb4128-66e9-4e90-936b-38dd8b5b8688SPL ID 5cdb4128-66e9-4e90-936b-38dd8b5b8688SPL set ID 04557ab3-6d21-49b4-b849-744c75b8a630RxCUI 1101775, 1101778UNII 4J9FJ0HL51
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N400486111101followed by a unit qualifier and the quantityPackage 00486-1111-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
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.
Excerpt only. Read the full label for complete information.
About NDC 0486-1111
- What is NDC 0486-1111?
- 0486-1111 is the product NDC for K Phos Original, Potassium phosphate, Monobasic 500 mg/1 tablet, soluble, listed with the FDA by Beach Products, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- K Phos Original (Potassium Phosphate, Monobasic).
- What is the active ingredient?
- Potassium phosphate, Monobasic.
- Who is the labeler?
- Beach Products, Inc., NDC labeler code 0486. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for K Phos Original?
- None: this is the only finished product listed under this name.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.