What is NDC 44911-0660?

44911-0660 is the product NDC for Organdrainex, Onion 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?

Organdrainex (Allium Cepa, Allium Sativum, Ambrosia Artemisiaefolia, Berberis Vulgaris, Chelidonium Majus, Collinsonia Canadensis, Cynara Scolymus, Petroselinum Sativum, Trifolium Pratense, Methylcobalamin, Aloe, Alpha-Lipoicum Acidum, Palladium Metallicum).

What is the active ingredient?

Onion, Garlic, Ambrosia artemisiifolia whole, Berberis vulgaris root bark, Chelidonium majus whole, Collinsonia canadensis root, Cynara scolymus leaf, Petroselinum crispum whole, Trifolium pratense flower, Methylcobalamin, Aloe, Alpha lipoic acid, Palladium.

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 Organdrainex?

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.

Organdrainex NDC 44911-0660 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0660Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0660Add 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
44911-0660-1	4491106600144911066001	118 mL in 1 BOTTLE, GLASS (44911-0660-1)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): Organdrainex
Generic name (nonproprietary): allium cepa, allium sativum, ambrosia artemisiaefolia, berberis vulgaris, chelidonium majus, collinsonia canadensis, cynara scolymus, petroselinum sativum, trifolium pratense, methylcobalamin, aloe, alpha-lipoicum acidum, palladium metallicum
Active ingredients: Onion — 3 [hp_X]/mLGarlic — 3 [hp_X]/mLAmbrosia artemisiifolia whole — 3 [hp_X]/mLBerberis vulgaris root bark — 3 [hp_X]/mLChelidonium majus whole — 3 [hp_X]/mLCollinsonia canadensis root — 3 [hp_X]/mLCynara scolymus leaf — 3 [hp_X]/mLPetroselinum crispum whole — 3 [hp_X]/mLTrifolium pratense flower — 3 [hp_X]/mLMethylcobalamin — 4 [hp_X]/mLAloe — 7 [hp_X]/mLAlpha lipoic acid — 12 [hp_X]/mLPalladium — 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: Oct 11, 2022
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 44911-0660_a1c8c4cd-54ab-4f10-8ef9-63428cdc72c5SPL ID a1c8c4cd-54ab-4f10-8ef9-63428cdc72c5SPL set ID 657065f2-b5c6-4036-a864-14169ddcd3bcUNII 492225Q21H, V1V998DC17, 9W34L2CQ9A, 1TH8Q20J0U, 7E889U5RNN, O2630F3XDR, B71UA545DE, 1WZA4Y92EX, 4JS0838828, BR1SN1JS2W, V5VD430YW9, 73Y7P0K73Y, 5TWQ1V240MUPC 0363113700213
Pharmacologic class: Non-Standardized Food Allergenic Extract

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

N444911066001 followed by a unit qualifier and the quantity

Package 44911-0660-01. 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 Jan 28, 2025.

Indications (excerpt from the label)

USES: May temporarily relieve symptoms associated with decreased lymphatic drainage of the organs, such as: •fatigue •headache •lymphatic swelling •bad effects from sedentary habits.** **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 44911-0660

What is NDC 44911-0660?: 44911-0660 is the product NDC for Organdrainex, Onion 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?: Organdrainex (Allium Cepa, Allium Sativum, Ambrosia Artemisiaefolia, Berberis Vulgaris, Chelidonium Majus, Collinsonia Canadensis, Cynara Scolymus, Petroselinum Sativum, Trifolium Pratense, Methylcobalamin, Aloe, Alpha-Lipoicum Acidum, Palladium Metallicum).
What is the active ingredient?: Onion, Garlic, Ambrosia artemisiifolia whole, Berberis vulgaris root bark, Chelidonium majus whole, Collinsonia canadensis root, Cynara scolymus leaf, Petroselinum crispum whole, Trifolium pratense flower, Methylcobalamin, Aloe, Alpha lipoic acid, Palladium.
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 Organdrainex?: 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.