Breathtone NDC 44911-0590

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0590Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0590Add 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
44911-0590-1	44911059001	30 mL in 1 BOTTLE, DROPPER (44911-0590-1)Marketed from May 27, 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): Breathtone
Generic name (nonproprietary): lobelia inflata, verbascum thapsus, balsamum peruvianum, antimonium tartaricum, arsenicum album, drosera (rotundifolia), kali bichromicum, kali carbonicum, natrum sulphuricum, phosphorous, spongia tosta
Active ingredients: Lobelia inflata whole — 3 [hp_X]/mLVerbascum thapsus whole — 3 [hp_X]/mLBalsam peru — 6 [hp_X]/mLAntimony potassium tartrate — 12 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLDrosera rotundifolia whole — 12 [hp_X]/mLPotassium dichromate — 12 [hp_X]/mLPotassium carbonate — 12 [hp_X]/mLSodium sulfate — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mLSpongia officinalis skeleton, Roasted — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 27, 2021
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)
Identifiers: Product ID 44911-0590_f5157189-1447-4dd3-b342-0c14ccaffcefSPL ID f5157189-1447-4dd3-b342-0c14ccaffcefSPL set ID c388da29-824a-41a5-be85-47a60bccf3daUNII 9PP1T3TC5U, C9TD27U172, 8P5F881OCY, DL6OZ476V3, S7V92P67HO, QR44N9XPJQ, T4423S18FM, BQN1B9B9HA, 0YPR65R21J, 27YLU75U4W, 1PIP394IIDUPC 0363113700688
Pharmacologic class: 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

N444911059001 followed by a unit qualifier and the quantity

Package 44911-0590-01. 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 Aug 14, 2023.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve dry hacking cough, hoarseness, bronchial congestion and hay fever symptoms, and difficulty breathing with tightness of chest from congestion of chest.** **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)