What is NDC 54973-5230?

54973-5230 is the product NDC for Kali Sulph (potassium sulfate), Potassium sulfate 6 [hp_X]/1 tablet, listed with the FDA by Hyland's Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Kali Sulph (Potassium sulfate).

Hyland's Inc., NDC labeler code 54973. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Kali Sulph?

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.

Kali Sulph NDC 54973-5230 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)54973-5230Labeler and product segments. Claims need a package NDC.

Product NDC at billing width54973-5230Add 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 NDC	11-digit (billing)	Package	Copy
54973-5230-1	5497352300154973523001	500 TABLET in 1 BOTTLE, PLASTIC (54973-5230-1)Marketed from Jan 1, 1940

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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): Kali Sulph
Generic name (nonproprietary): potassium sulfate
Active ingredients: Potassium sulfate — 6 [hp_X]/1
Dosage form: Tablet
Route: Oral
Labeler: Hyland's Inc.NDC labeler code 54973
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 1, 1940
Listing expires: Dec 31, 2026
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)
Identifiers: Product ID 54973-5230_f0330ffb-503d-2671-e053-2995a90a8218SPL ID f0330ffb-503d-2671-e053-2995a90a8218SPL set ID c00e31d8-76df-47b1-bafd-36d088395522UNII 1K573LC5TVUPC 0354973523012
Pharmacologic class: Osmotic Laxative

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

N454973523001 followed by a unit qualifier and the quantity

Package 54973-5230-01. 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 Dec 19, 2022.

Indications (excerpt from the label)

INDICATIONS Relief of symptoms of the common cold. Relief of symptoms of pimples and blemishes associated with common acne.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 54973-5230

What is NDC 54973-5230?: 54973-5230 is the product NDC for Kali Sulph (potassium sulfate), Potassium sulfate 6 [hp_X]/1 tablet, listed with the FDA by Hyland's Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Kali Sulph (Potassium sulfate).
What is the active ingredient?: Potassium sulfate.
Who is the labeler?: Hyland's Inc., NDC labeler code 54973. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Kali Sulph?: 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.

Kali Sulph (Potassium sulfate) NDC 54973-5230