What is NDC 44911-0591?

44911-0591 is the product NDC for Breath HP, Ammonium chloride 30 [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?

Breath HP (Ammonium Muriaticum, Antimonium Tartaricum, Arsenicum Album, Bryonia (Alba), Calcarea Carbonica, Lobelia Inflata, Natrum Sulphuricum, Phosphorus, Spongia Tosta).

What is the active ingredient?

Ammonium chloride, Antimony potassium tartrate, Arsenic trioxide, Bryonia alba root, Oyster shell calcium carbonate, Crude, Lobelia inflata whole, Sodium sulfate, Phosphorus, Spongia officinalis skeleton, Roasted.

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 Breath HP?

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.

Breath HP NDC 44911-0591 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0591Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0591Add 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
44911-0591-1	4491105910144911059101	30 mL in 1 BOTTLE, DROPPER (44911-0591-1)Marketed from Jun 1, 2021

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): Breath HP
Generic name (nonproprietary): ammonium muriaticum, antimonium tartaricum, arsenicum album, bryonia (alba), calcarea carbonica, lobelia inflata, natrum sulphuricum, phosphorus, spongia tosta
Active ingredients: Ammonium chloride — 30 [hp_X]/mLAntimony potassium tartrate — 30 [hp_X]/mLArsenic trioxide — 30 [hp_X]/mLBryonia alba root — 30 [hp_X]/mLOyster shell calcium carbonate, Crude — 30 [hp_X]/mLLobelia inflata whole — 30 [hp_X]/mLSodium sulfate — 30 [hp_X]/mLPhosphorus — 30 [hp_X]/mLSpongia officinalis skeleton, Roasted — 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 1, 2021
Listing expires: Dec 31, 2026
Identifiers: Product ID 44911-0591_7ef692ed-d44b-414e-8297-e157ac76e66fSPL ID 7ef692ed-d44b-414e-8297-e157ac76e66fSPL set ID f487452a-e3de-4cd1-bda7-90b6b4daf971UNII 01Q9PC255D, DL6OZ476V3, S7V92P67HO, T7J046YI2B, 2E32821G6I, 9PP1T3TC5U, 0YPR65R21J, 27YLU75U4W, 1PIP394IID

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

N444911059101 followed by a unit qualifier and the quantity

Package 44911-0591-01. 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 Jul 23, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve productive cough, chest congestion, shortness of breath and Fatigue.** **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 44911-0591

What is NDC 44911-0591?: 44911-0591 is the product NDC for Breath HP, Ammonium chloride 30 [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?: Breath HP (Ammonium Muriaticum, Antimonium Tartaricum, Arsenicum Album, Bryonia (Alba), Calcarea Carbonica, Lobelia Inflata, Natrum Sulphuricum, Phosphorus, Spongia Tosta).
What is the active ingredient?: Ammonium chloride, Antimony potassium tartrate, Arsenic trioxide, Bryonia alba root, Oyster shell calcium carbonate, Crude, Lobelia inflata whole, Sodium sulfate, Phosphorus, Spongia officinalis skeleton, Roasted.
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 Breath HP?: 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.