Hthy NDC 62106-0631

NDC codes

FDA NDC Directory

Product NDC (as listed)62106-0631Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62106-0631Add 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
62106-0631-0	62106063100	1 BOTTLE, GLASS in 1 CARTON (62106-0631-0) / 30 mL in 1 BOTTLE, GLASSMarketed from Nov 27, 2015

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): Hthy
Generic name (nonproprietary): calcarea carbonica, calcarea iodata, ferrum iodatum, fucus vesiculosus, hepar sulphuris calcareum, kali iodatum, lapis albus calcium fluosilicate, oryctolagus cuniculus (rabbit) adrenal gland, oryctolagus cuniculus (rabbit) pituitary gland, oryctolagus cuniculus (rabbit) spleen, oryctolagus cuniculus (rabbit) thymus gland, oryctolagus cuniculus (rabbit) thyroid gland, spongia tosta
Active ingredients: Oyster shell calcium carbonate, Crude — 8 [hp_X]/30mLCalcium iodide — 4 [hp_X]/30mLFerrous iodide — 6 [hp_X]/30mLFucus vesiculosus — 6 [hp_X]/30mLCalcium sulfide — 8 [hp_X]/30mLCalcium hexafluorosilicate — 6 [hp_X]/30mLOryctolagus cuniculus adrenal gland — 10 [hp_X]/30mLOryctolagus cuniculus pituitary gland — 10 [hp_X]/30mLOryctolagus cuniculus spleen — 10 [hp_X]/30mLOryctolagus cuniculus thymus — 10 [hp_X]/30mLSpongia officinalis skeleton, Roasted — 6 [hp_X]/30mLPotassium iodide — 6 [hp_X]/30mLOryctolagus cuniculus thyroid — 10 [hp_X]/30mL
Dosage form: Liquid
Route: Oral
Labeler: Seroyal USA
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Nov 27, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Calcium (Chemical structure)Divalent (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)
Identifiers: Product ID 62106-0631_f382fc1f-d3b7-7fa7-e053-2995a90a0eabSPL ID f382fc1f-d3b7-7fa7-e053-2995a90a0eabSPL set ID 079bede5-f618-03ed-e054-00144ff8d46cUNII 2E32821G6I, 8EKI9QEE2H, F5452U54PN, 535G2ABX9M, 1MBW07J51Q, 2NVP93XVQ3, QGY289M89Q, T9F9ZW799A, 01WNS05SFO, 7ZO132YX2X, 1PIP394IID, 1C4QK22F9J, 97K9E28344UPC 0883196138104
Pharmacologic class: Blood Coagulation Factor

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

N462106063100 followed by a unit qualifier and the quantity

Package 62106-0631-00. 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 30, 2023.

Indications (excerpt from the label)

Uses Helps promote and maintain normal metabolic functions. Directions To be taken 20 minutes away from food. Place drops directly under the tongue or into ¼ oz of water. Adults and adolescents (12 years and older): Take 10 drops two to three 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.

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