Cough Relief Syrup NDC 66096-709

NDC codes

FDA NDC Directory

Product NDC (as listed)66096-709Labeler and product segments. Claims need a package NDC.

Product NDC at billing width66096-0709Add 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
66096-709-25	66096070925	148 mL in 1 BOTTLE (66096-709-25)Marketed from Aug 18, 2015

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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 Relief Syrup
Generic name (nonproprietary): althaea, antimon sulph, antimon tart, bryonia, cetraria, chamomilla, drosera, echinacea ang, ipecac, kali mur, plantago, rumex crisp, senega, spongia, thymus, trifolium prat, urtica di, verbascum.
Active ingredients: Althaea officinalis root — 1 [hp_X]/148mLAntimony pentasulfide — 12 [hp_X]/148mLAntimony potassium tartrate — 6 [hp_X]/148mLBryonia alba root — 6 [hp_X]/148mLCetraria islandica subsp. Islandica — 1 [hp_X]/148mLMatricaria recutita — 1 [hp_X]/148mLDrosera rotundifolia — 6 [hp_X]/148mLEchinacea angustifolia — 1 [hp_X]/148mLIpecac — 6 [hp_X]/148mLPotassium chloride — 6 [hp_X]/148mLPlantago lanceolata pollen — 1 [hp_X]/148mLRumex crispus root — 6 [hp_X]/148mLPolygala senega root — 6 [hp_X]/148mLSpongia officinalis skeleton, Roasted — 6 [hp_X]/148mLSus scrofa thymus — 1 [hp_X]/148mLTrifolium pratense flower — 1 [hp_X]/148mLUrtica dioica — 1 [hp_X]/148mLVerbascum thapsus — 1 [hp_X]/148mL
Dosage form: Liquid
Route: Oral
Labeler: OHM PHARMA INC.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 18, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Pollen (Chemical structure)Potassium Compounds (Chemical structure)
Identifiers: Product ID 66096-709_d44af2b7-f77f-3d27-e053-2a95a90abc46SPL ID d44af2b7-f77f-3d27-e053-2a95a90abc46SPL set ID 5285cdbb-8502-4ff4-977a-cb3c5ae2cc9bUNII TRW2FUF47H, 1433F1I86N, DL6OZ476V3, T7J046YI2B, BJ7YPN79A1, G0R4UBI2ZZ, QR44N9XPJQ, VB06AV5US8, 62I3C8233L, 660YQ98I10, DO87T1U2CI, 9N1RM2S62C, M7T6H7D4IF, 1PIP394IID, 7B69B0BD62, 4JS0838828, 710FLW4U46, C9TD27U172UPC 0366096709259
Pharmacologic class: Non-Standardized Pollen Allergenic Extract; Osmotic Laxative; Potassium Salt

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

N466096070925 followed by a unit qualifier and the quantity

Package 66096-0709-25. 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 Dec 29, 2021.

Indications (excerpt from the label)

USES: Temporarily relieves cough symptoms of diverse origins. Loosens chest congestion facilitating a productive cough. Soothes dry cough due to throat and bronquial irritation.** * *This statement has not been evaluated by the FDA. It is based on documented Homeopathic Materia Medica.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)