What is NDC 44911-0439?

44911-0439 is the product NDC for Lungex II, Ginkgo 6 [hp_X]/mL + 19 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?

Lungex II (Ginkgo Biloba, Colon (Suis), Lung (Suis), Pancreas Suis, Germanium Sesquioxide, Cuprum Metallicum, Manganum Metallicum, Stannum Metallicum, alpha-Ketoglutaricum Acidum, Citricum Acidum, Fumaricum Acidum, Malic Acid, Pyruvic Acid, Succinicum Acidum, Naphthoquinone, Arsenicum Metallicum, Calcarea Carbonica, Aconiticum Acidum, Cis, Natrum Oxalaceticum, Phosphorus).

What is the active ingredient?

Ginkgo, Sus scrofa colon, Sus scrofa lung, Sus scrofa pancreas, Germanium sesquioxide, Copper, Manganese, Tin, Oxogluric acid, Citric acid monohydrate, Fumaric acid, Malic acid, Pyruvic acid, Succinic acid, 1,2-naphthoquinone, Arsenic, Oyster shell calcium carbonate, Crude, Aconitic acid, Sodium diethyl oxalacetate, 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 Lungex II?

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.

Lungex II NDC 44911-0439 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0439Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0439Add 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
44911-0439-1	44911043901	30 mL in 1 BOTTLE, DROPPER (44911-0439-1)Marketed from Sep 8, 2017

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): Lungex IISuffix: II
Generic name (nonproprietary): ginkgo biloba, colon (suis), lung (suis), pancreas suis, germanium sesquioxide, cuprum metallicum, manganum metallicum, stannum metallicum, alpha-ketoglutaricum acidum, citricum acidum, fumaricum acidum, malic acid, pyruvic acid, succinicum acidum, naphthoquinone, arsenicum metallicum, calcarea carbonica, aconiticum acidum, cis, natrum oxalaceticum, phosphorus
Active ingredients: Ginkgo — 6 [hp_X]/mLSus scrofa colon — 6 [hp_X]/mLSus scrofa lung — 6 [hp_X]/mLSus scrofa pancreas — 6 [hp_X]/mLGermanium sesquioxide — 8 [hp_X]/mLCopper — 8 [hp_X]/mLManganese — 8 [hp_X]/mLTin — 8 [hp_X]/mLOxogluric acid — 8 [hp_X]/mLCitric acid monohydrate — 8 [hp_X]/mLFumaric acid — 8 [hp_X]/mLMalic acid — 8 [hp_X]/mLPyruvic acid — 8 [hp_X]/mLSuccinic acid — 8 [hp_X]/mL1,2-naphthoquinone — 9 [hp_X]/mLArsenic — 12 [hp_X]/mLOyster shell calcium carbonate, Crude — 12 [hp_X]/mLAconitic acid — 12 [hp_X]/mLSodium diethyl oxalacetate — 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: Sep 8, 2017
Listing expires: Dec 31, 2026
Other FDA classes: Acidifying Activity (Mechanism)Calcium Chelating Activity (Mechanism)Copper (Chemical structure)Decreased Coagulation Factor Activity (Physiologic effect)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)
Identifiers: Product ID 44911-0439_6b5ca9cb-ad13-44ab-a49f-4d569a01f6a7SPL ID 6b5ca9cb-ad13-44ab-a49f-4d569a01f6a7SPL set ID ddf7fc46-95b7-44b4-b7ca-96a066a3fa2bUNII 19FUJ2C58T, 94J255A0UC, 7GL3G1COB3, 9Y3J3362RY, 96WE91N25T, 789U1901C5, 42Z2K6ZL8P, 387GMG9FH5, 8ID597Z82X, 2968PHW8QP, 88XHZ13131, 817L1N4CKP, 8558G7RUTR, AB6MNQ6J6L, 804K62F61Q, N712M78A8G, 2E32821G6I, 93371T1BXP, 6CA025Y4FG, 27YLU75U4WUPC 0363113701043
Pharmacologic class: Anti-coagulant; Calculi Dissolution Agent; Copper-containing Intrauterine Device

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

N444911043901 followed by a unit qualifier and the quantity

Package 44911-0439-01. 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 28, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve coughing, wheezing, diarrhea, abdominal pain, and bloating.** **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 44911-0439

What is NDC 44911-0439?: 44911-0439 is the product NDC for Lungex II, Ginkgo 6 [hp_X]/mL + 19 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?: Lungex II (Ginkgo Biloba, Colon (Suis), Lung (Suis), Pancreas Suis, Germanium Sesquioxide, Cuprum Metallicum, Manganum Metallicum, Stannum Metallicum, alpha-Ketoglutaricum Acidum, Citricum Acidum, Fumaricum Acidum, Malic Acid, Pyruvic Acid, Succinicum Acidum, Naphthoquinone, Arsenicum Metallicum, Calcarea Carbonica, Aconiticum Acidum, Cis, Natrum Oxalaceticum, Phosphorus).
What is the active ingredient?: Ginkgo, Sus scrofa colon, Sus scrofa lung, Sus scrofa pancreas, Germanium sesquioxide, Copper, Manganese, Tin, Oxogluric acid, Citric acid monohydrate, Fumaric acid, Malic acid, Pyruvic acid, Succinic acid, 1,2-naphthoquinone, Arsenic, Oyster shell calcium carbonate, Crude, Aconitic acid, Sodium diethyl oxalacetate, 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 Lungex II?: 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.