Cough plus Bronchial NDC 50845-0246

NDC codes

FDA NDC Directory

Product NDC (as listed)50845-0246Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50845-0246Add 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
50845-0246-1	50845024601	30 mL in 1 BOTTLE, SPRAY (50845-0246-1)Marketed from Apr 9, 2019

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): Cough plus Bronchial
Generic name (nonproprietary): antimonium tartaricum, arum triphyllum, badiaga, baptisia tinctoria, bryonia (alba), drosera (rotundifolia), echinacea (angustifolia), eupatorium perfoliatum, kali bromatum, lung suis, phosphorus, pulsatilla (pratensis), spongia tosta, sticta pulmonaria, sulphur iodatum, urtica urens
Active ingredients: Antimony potassium tartrate — 200 [hp_C]/mLArisaema triphyllum root — 30 [hp_C]/mLSpongilla lacustris — 12 [hp_X]/mLBaptisia tinctoria root — 3 [hp_X]/mLBryonia alba root — 200 [hp_C]/mLDrosera rotundifolia whole — 3 [hp_X]/mLEchinacea angustifolia whole — 3 [hp_X]/mLEupatorium perfoliatum flowering top — 200 [hp_C]/mLPotassium bromide — 6 [hp_X]/mLSus scrofa lung — 6 [hp_X]/mLPhosphorus — 30 [hp_C]/mLPulsatilla pratensis whole — 30 [hp_C]/mLSilicon dioxide — 12 [hp_X]/mLSpongia officinalis skeleton, Roasted — 12 [hp_X]/mLLobaria pulmonaria — 200 [hp_C]/mLSulfur iodide — 200 [hp_C]/mLUrtica urens whole — 200 [hp_C]/mL
Dosage form: Spray
Route: Oral
Labeler: Liddell Laboratories, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Apr 9, 2019
Listing expires: Dec 31, 2026
Identifiers: Product ID 50845-0246_f7a1859f-8cf8-4dd7-9497-ddc26a9f5388SPL ID f7a1859f-8cf8-4dd7-9497-ddc26a9f5388SPL set ID 801eba42-4217-46e9-8f3e-745da01a27b0UNII DL6OZ476V3, DM64K844DM, 6SZ0G98BHM, 5EF0HWI5WU, T7J046YI2B, QR44N9XPJQ, VB06AV5US8, 1W0775VX6E, OSD78555ZM, 7GL3G1COB3, 27YLU75U4W, 8E272251DI, ETJ7Z6XBU4, 1PIP394IID, D1YM0P5Z2T, L6L8KA2AA0, IHN2NQ5OF9

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

N450845024601 followed by a unit qualifier and the quantity

Package 50845-0246-01. 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 1, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve these symptoms associated with cough and bronchial congestion: • coughing • mucous buildup • chest tightness • chest soreness** **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)