What is NDC 44911-0465?

44911-0465 is the product NDC for Circulapar, Selenicereus grandiflorus stem 3 [hp_X]/mL + 12 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?

Circulapar (Cactus Grandiflorus, Hamamelis Virginiana, Valeriana Officinalis, Arteria Suis, Heart (Suis), Arnica Montana, Aurum Metallicum, Baryta Muriatica, Cholesterinum, Lecithin, Magnesia Muriatica, Oxalicum Acidum, Phosphorus).

What is the active ingredient?

Selenicereus grandiflorus stem, Hamamelis virginiana root bark/stem bark, Valerian, Sus scrofa artery, Pork heart, Arnica montana whole, Gold, Barium chloride dihydrate, Cholesterol, Soybean lecithin, Magnesium chloride, Oxalic acid, Phosphorus.

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 Circulapar?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Circulapar NDC 44911-0465 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0465Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0465Add 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
44911-0465-1	4491104650144911046501	30 mL in 1 BOTTLE, DROPPER (44911-0465-1)Marketed from Aug 16, 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): Circulapar
Generic name (nonproprietary): cactus grandiflorus, hamamelis virginiana, valeriana officinalis, arteria suis, heart (suis), arnica montana, aurum metallicum, baryta muriatica, cholesterinum, lecithin, magnesia muriatica, oxalicum acidum, phosphorus
Active ingredients: Selenicereus grandiflorus stem — 3 [hp_X]/mLHamamelis virginiana root bark/stem bark — 3 [hp_X]/mLValerian — 3 [hp_X]/mLSus scrofa artery — 8 [hp_X]/mLPork heart — 8 [hp_X]/mLArnica montana whole — 12 [hp_X]/mLGold — 12 [hp_X]/mLBarium chloride dihydrate — 12 [hp_X]/mLCholesterol — 12 [hp_X]/mLSoybean lecithin — 12 [hp_X]/mLMagnesium chloride — 12 [hp_X]/mLOxalic acid — 12 [hp_X]/mLPhosphorus — 12 [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: Aug 16, 2018
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)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 44911-0465_1d6a00c8-c120-47c1-9349-8c0a820f6964SPL ID 1d6a00c8-c120-47c1-9349-8c0a820f6964SPL set ID 5bc2bcd0-5687-462a-8701-37c904a2e2d0UNII 7114SV0MYK, T7S323PKJS, JWF5YAW3QW, 63O327782Q, X876KJM95L, O80TY208ZW, 79Y1949PYO, EL5GJ3U77E, 97C5T2UQ7J, 1DI56QDM62, 02F3473H9O, 9E7R5L6H31, 27YLU75U4WUPC 0363113701364
Pharmacologic class: Calculi Dissolution Agent; Osmotic Laxative; Standardized Chemical Allergen

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

N444911046501 followed by a unit qualifier and the quantity

Package 44911-0465-01. 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 24, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve cold clammy feet, numbness of limbs, painful calves upon walking, and muscular weakness of the lower extremities.** **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 44911-0465

What is NDC 44911-0465?: 44911-0465 is the product NDC for Circulapar, Selenicereus grandiflorus stem 3 [hp_X]/mL + 12 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?: Circulapar (Cactus Grandiflorus, Hamamelis Virginiana, Valeriana Officinalis, Arteria Suis, Heart (Suis), Arnica Montana, Aurum Metallicum, Baryta Muriatica, Cholesterinum, Lecithin, Magnesia Muriatica, Oxalicum Acidum, Phosphorus).
What is the active ingredient?: Selenicereus grandiflorus stem, Hamamelis virginiana root bark/stem bark, Valerian, Sus scrofa artery, Pork heart, Arnica montana whole, Gold, Barium chloride dihydrate, Cholesterol, Soybean lecithin, Magnesium chloride, Oxalic acid, Phosphorus.
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 Circulapar?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.