Kalium Sulfuricum 6X (potassium sulfate) NDC 62106-1056

NDC codes

FDA NDC Directory

Product NDC (as listed)62106-1056Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62106-1056Add 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
62106-1056-2	62106105602	1 BOTTLE, GLASS in 1 CARTON (62106-1056-2) / 100 TABLET in 1 BOTTLE, GLASSMarketed from May 3, 2018

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): Kalium Sulfuricum 6X
Generic name (nonproprietary): potassium sulfate
Active ingredients: Potassium sulfate — 6 [hp_X]/1
Dosage form: Tablet
Route: Sublingual
Labeler: Seroyal USA
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 3, 2018
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)Potassium Compounds (Chemical structure)
Identifiers: Product ID 62106-1056_e33c9914-4d57-0790-e053-2a95a90a79e8SPL ID e33c9914-4d57-0790-e053-2a95a90a79e8SPL set ID 6b5443ce-fc30-04e3-e053-2991aa0a5ab6UNII 1K573LC5TV
Pharmacologic class: Osmotic Laxative; Potassium Salt

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. Sublingual products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N462106105602 followed by a unit qualifier and the quantity

Package 62106-1056-02. 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 Jul 7, 2022.

Indications (excerpt from the label)

Uses For the temporary relief of minor symptoms associated with minor skin irritation. Directions Tip bottle slightly allowing for tablets to fall into the cap. Use cap to drop tablets into mouth and allow them to dissolve under the tongue. Adults and adolescents (12 years and older) Take 1 to 4 tablets, one to four times daily, or as recommended by your healthcare practitioner. Children (under 12 years) Take under the direction of your healthcare practitioner.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)