What is NDC 44911-0675?

44911-0675 is the product NDC for Anxiety HP, Aconitum napellus whole 30 [hp_X]/mL + 11 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?

Anxiety HP (Aconitum Napellus, Argentum Nitricum, Arsenicum Album, Calcarea Carbonica, Ignatia Amara, Kali Carbonicum, Lachesis Mutus, Natrum Muriaticum, Phosphorus, Pulsatilla (Pratensis), Staphysagria, Stramonium).

What is the active ingredient?

Aconitum napellus whole, Silver nitrate, Arsenic trioxide, Oyster shell calcium carbonate, Crude, Strychnos ignatii seed, Potassium carbonate, Lachesis muta venom, Sodium chloride, Phosphorus, Pulsatilla pratensis whole, Delphinium staphisagria seed, Datura stramonium.

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 Anxiety HP?

1 other product NDC are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Anxiety HP NDC 44911-0675 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0675Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0675Add 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
44911-0675-1	4491106750144911067501	30 mL in 1 BOTTLE, DROPPER (44911-0675-1)Marketed from Jun 9, 2023

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): Anxiety HPSuffix: HP
Generic name (nonproprietary): aconitum napellus, argentum nitricum, arsenicum album, calcarea carbonica, ignatia amara, kali carbonicum, lachesis mutus, natrum muriaticum, phosphorus, pulsatilla (pratensis), staphysagria, stramonium
Active ingredients: Aconitum napellus whole — 30 [hp_X]/mLSilver nitrate — 30 [hp_X]/mLArsenic trioxide — 30 [hp_X]/mLOyster shell calcium carbonate, Crude — 30 [hp_X]/mLStrychnos ignatii seed — 30 [hp_X]/mLPotassium carbonate — 30 [hp_X]/mLLachesis muta venom — 30 [hp_X]/mLSodium chloride — 30 [hp_X]/mLPhosphorus — 30 [hp_X]/mLPulsatilla pratensis whole — 30 [hp_X]/mLDelphinium staphisagria seed — 30 [hp_X]/mLDatura stramonium — 30 [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: Jun 9, 2023
Listing expires: Dec 31, 2026
Identifiers: Product ID 44911-0675_e471248f-71c3-492f-88ea-072eb4483945SPL ID e471248f-71c3-492f-88ea-072eb4483945SPL set ID 191393fa-5f36-43c0-a183-09258eef9bdaUNII U0NQ8555JD, 95IT3W8JZE, S7V92P67HO, 2E32821G6I, 1NM3M2487K, BQN1B9B9HA, VSW71SS07I, 451W47IQ8X, 27YLU75U4W, 8E272251DI, 00543AP1JV, G6W4F0V8Z3UPC 0363113701371

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

N444911067501 followed by a unit qualifier and the quantity

Package 44911-0675-01. 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 Mar 20, 2025.

Indications (excerpt from the label)

USES: May temporarily relieve symptoms of: •anxiety nervousness. ** **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 44911-0675

What is NDC 44911-0675?: 44911-0675 is the product NDC for Anxiety HP, Aconitum napellus whole 30 [hp_X]/mL + 11 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?: Anxiety HP (Aconitum Napellus, Argentum Nitricum, Arsenicum Album, Calcarea Carbonica, Ignatia Amara, Kali Carbonicum, Lachesis Mutus, Natrum Muriaticum, Phosphorus, Pulsatilla (Pratensis), Staphysagria, Stramonium).
What is the active ingredient?: Aconitum napellus whole, Silver nitrate, Arsenic trioxide, Oyster shell calcium carbonate, Crude, Strychnos ignatii seed, Potassium carbonate, Lachesis muta venom, Sodium chloride, Phosphorus, Pulsatilla pratensis whole, Delphinium staphisagria seed, Datura stramonium.
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 Anxiety HP?: 1 other product NDC are listed under this name. See all Anxiety HP 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 Anxiety HP NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Anxiety HParsenic trioxide, calcium carbonate, strychnos ignatii seed, potassium carbonate, lachesis muta venom, sodium chloride, phosphorus, pulsatilla	Arsenic trioxide 30 [hp_X]/mL + 7 more ingredients	LiquidOral	Natural Creations, Inc.	43406-0003	43406-0003-01