NDC codes

FDA NDC Directory
Product NDC (as listed)0486-1111Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00486-1111Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
0486-1111-010048611110100486111101100 TABLET, SOLUBLE in 1 BOTTLE (0486-1111-01)Marketed from Mar 29, 1977
0486-1111-050048611110500486111105500 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

N400486111101 followed by a unit qualifier and the quantity

Package 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.

Full label on DailyMed (opens in a new tab)

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.

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