co-HYPERT NDC 59469-304

NDC codes

FDA NDC Directory

Product NDC (as listed)59469-304Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59469-0304Add 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
59469-304-10	59469030410	1 BOTTLE, GLASS in 1 BOX (59469-304-10) / 50 mL in 1 BOTTLE, GLASSMarketed from Jun 24, 2019

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): co-HYPERT
Generic name (nonproprietary): sodium tetrachloroaurate, barium carbonate, anamirta cocculus seed, iberis amara seed, magnesium chloride, ferula sumbul root, melilotus officinalis top, and viscum album fruiting top
Active ingredients: Sodium tetrachloroaurate — 6 [hp_X]/50mLBarium carbonate — 8 [hp_X]/50mLAnamirta cocculus seed — 4 [hp_X]/50mLIberis amara seed — 4 [hp_X]/50mLMagnesium chloride — 6 [hp_X]/50mLFerula sumbul root — 6 [hp_X]/50mLMelilotus officinalis top — 3 [hp_X]/50mLViscum album fruiting top — 3 [hp_X]/50mL
Dosage form: Solution/ drops
Route: Oral
Labeler: PEKANA Naturheilmittel Gmbh
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 24, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 59469-304_a68d96c9-c25c-48db-b807-9628b9721117SPL ID a68d96c9-c25c-48db-b807-9628b9721117SPL set ID 19ba62c0-2c49-47c4-9406-0e637df04b75UNII 7FT6QUT299, 6P669D8HQ8, 810258W28U, T90A7M66YF, 02F3473H9O, GLA4808EHQ, GM6P02J2DX, BK9092J5MP
Pharmacologic class: Calculi Dissolution Agent; 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

N459469030410 followed by a unit qualifier and the quantity

Package 59469-0304-10. 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 Jan 11, 2023.

Indications (excerpt from the label)

Indications For relief of occasional nervous tension. Application of this homeopathic remedy for the designated usage is exclusively based on homeopathic experience. With severe forms of this disease, a clinically proven therapy is indicated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)