What is NDC 44911-0711?

44911-0711 is the product NDC for Osteopar, Equisetum hyemale whole 3 [hp_X]/mL + 8 more ingredients liquid, listed with the FDA by Energique, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Osteopar (Equisetum Hyemale, Symphytum Officinale, Calcarea Carbonica, Calcarea Fluorica, Calcarea Phosphorica, Medulla Ossis Suis, Oleum Morrhuae, Silicea, Hekla Lava).

What is the active ingredient?

Equisetum hyemale whole, Comfrey root, Oyster shell calcium carbonate, Crude, Calcium fluoride, Tribasic calcium phosphate, Sus scrofa bone marrow, Cod liver oil, Silicon dioxide, Hekla lava.

Energique, Inc., NDC labeler code 44911. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Osteopar?

1 other product NDC are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Osteopar NDC 44911-0711 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0711Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0711Add 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
44911-0711-1	4491107110144911071101	30 mL in 1 BOTTLE, DROPPER (44911-0711-1)Marketed from May 21, 2024

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): Osteopar
Generic name (nonproprietary): equisetum hyemale, symphytum officinale, calcarea carbonica, calcarea fluorica, calcarea phosphorica, medulla ossis suis, oleum morrhuae, silicea, hekla lava
Active ingredients: Equisetum hyemale whole — 3 [hp_X]/mLComfrey root — 6 [hp_X]/mLOyster shell calcium carbonate, Crude — 12 [hp_X]/mLCalcium fluoride — 12 [hp_X]/mLTribasic calcium phosphate — 12 [hp_X]/mLSus scrofa bone marrow — 12 [hp_X]/mLCod liver oil — 12 [hp_X]/mLSilicon dioxide — 12 [hp_X]/mLHekla lava — 15 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.NDC labeler code 44911
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 21, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Calcium (Chemical structure)Divalent (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Phosphate Chelating Activity (Mechanism)
Identifiers: Product ID 44911-0711_aecc0eab-0618-415e-b035-8f971ecd453cSPL ID aecc0eab-0618-415e-b035-8f971ecd453cSPL set ID 6c346a26-26a2-4be0-b8a3-bbb5709bcf3dUNII 59677RXH25, M9VVZ08EKQ, 2E32821G6I, O3B55K4YKI, 91D9GV0Z28, VP2CN2G7Y8, BBL281NWFG, ETJ7Z6XBU4, C21158IIRKUPC 0363113701081
Pharmacologic class: Blood Coagulation Factor; Phosphate Binder

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

N444911071101 followed by a unit qualifier and the quantity

Package 44911-0711-01. 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 May 21, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve pain in lower back with burning, soreness in the sacroiliac area, and pain in the joints and bones.** **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)

About NDC 44911-0711

What is NDC 44911-0711?: 44911-0711 is the product NDC for Osteopar, Equisetum hyemale whole 3 [hp_X]/mL + 8 more ingredients liquid, listed with the FDA by Energique, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Osteopar (Equisetum Hyemale, Symphytum Officinale, Calcarea Carbonica, Calcarea Fluorica, Calcarea Phosphorica, Medulla Ossis Suis, Oleum Morrhuae, Silicea, Hekla Lava).
What is the active ingredient?: Equisetum hyemale whole, Comfrey root, Oyster shell calcium carbonate, Crude, Calcium fluoride, Tribasic calcium phosphate, Sus scrofa bone marrow, Cod liver oil, Silicon dioxide, Hekla lava.
Who is the labeler?: Energique, Inc., NDC labeler code 44911. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Osteopar?: 1 other product NDC are listed under this name. See all Osteopar NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Osteopar NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Osteoparequisetum hyemale, symphytum officinale, calcarea carbonica, calcarea fluorica, calcarea phosphorica, medulla ossis suis, ossa sepia, silicea, hekla lava	Equisetum hyemale whole 3 [hp_X]/mL + 8 more ingredients	LiquidOral	Energique, Inc.	44911-0367	44911-0367-01