Spinapar NDC 44911-0659

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0659Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0659Add 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
44911-0659-1	44911065901	30 mL in 1 BOTTLE, DROPPER (44911-0659-1)Marketed from Oct 11, 2022

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): Spinapar
Generic name (nonproprietary): aesculus hippocastanum, harpagophytum, phytolacca decandra, ruta graveolens, cartilago suis, discus intervertebralis suis, agaricus muscarius, argentum metallicum, arnica montana, bambusa arundinacea, bellis perennis, bryonia (alba), calcarea fluorica, hypericum perforatum, rhus tox, sulphur, tellurium metallicum
Active ingredients: Horse chestnut — 4 [hp_X]/mLHarpagophytum procumbens root — 4 [hp_X]/mLPhytolacca americana root — 4 [hp_X]/mLRuta graveolens flowering top — 4 [hp_X]/mLSus scrofa cartilage — 6 [hp_X]/mLSus scrofa intervertebral disc — 6 [hp_X]/mLAmanita muscaria fruiting body — 12 [hp_X]/mLSilver — 12 [hp_X]/mLArnica montana whole — 12 [hp_X]/mLBambusa bambos leaf — 12 [hp_X]/mLBambusa bambos sap — 12 [hp_X]/mLBellis perennis whole — 12 [hp_X]/mLBryonia alba root — 12 [hp_X]/mLCalcium fluoride — 12 [hp_X]/mLHypericum perforatum whole — 12 [hp_X]/mLToxicodendron pubescens leaf — 12 [hp_X]/mLSulfur — 12 [hp_X]/mLTellurium — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 11, 2022
Listing expires: Dec 31, 2026
Identifiers: Product ID 44911-0659_fefaacf7-d239-4245-916e-49d748c75ea5SPL ID fefaacf7-d239-4245-916e-49d748c75ea5SPL set ID e3e1da2e-965b-4be7-a43d-a6cef4692248UNII 3C18L6RJAZ, 1OYM338E89, 11E6VI8VEG, N94C2U587S, 73ECW5WG2F, OJ17O2WTSM, DIF093I037, 3M4G523W1G, O80TY208ZW, HW86D1FGSS, DPQ0BJD6MR, 2HU33I03UY, T7J046YI2B, O3B55K4YKI, XK4IUX8MNB, 6IO182RP7A, 70FD1KFU70, NQA0O090ZJUPC 0363113701760

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

N444911065901 followed by a unit qualifier and the quantity

Package 44911-0659-01. 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 Oct 30, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve minor back pain, stiffness, numbness or tingling.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)