Cough Relief NDC 66096-115

NDC codes

FDA NDC Directory

Product NDC (as listed)66096-115Labeler and product segments. Claims need a package NDC.

Product NDC at billing width66096-0115Add 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
66096-115-05	66096011505	59 mL in 1 BOTTLE, SPRAY (66096-115-05)Marketed from May 21, 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
Generic name (nonproprietary): aconitum nap, antimon crud, antimon sulph, antimon tart, aralia rac, bryonia, chelidonium maj, cuprum met, drosera, hepar sulph calc, kali carb, spongia.
Active ingredients: Aconitum napellus — 6 [hp_X]/59mLAntimony trisulfide — 8 [hp_X]/59mLAntimony pentasulfide — 8 [hp_X]/59mLAntimony potassium tartrate — 8 [hp_X]/59mLAralia racemosa root — 4 [hp_X]/59mLBryonia alba root — 6 [hp_X]/59mLChelidonium majus — 6 [hp_X]/59mLCopper — 12 [hp_X]/59mLDrosera rotundifolia — 6 [hp_X]/59mLCalcium sulfide — 12 [hp_X]/59mLPotassium carbonate — 12 [hp_X]/59mLSpongia officinalis skeleton, Roasted — 6 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: OHM PHARMA INC.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 21, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)
Identifiers: Product ID 66096-115_d44af2b7-f773-3d27-e053-2a95a90abc46SPL ID d44af2b7-f773-3d27-e053-2a95a90abc46SPL set ID 991fd747-7a46-4689-afac-381c57b91e05UNII U0NQ8555JD, F79059A38U, 1433F1I86N, DL6OZ476V3, T90W4582DU, T7J046YI2B, 7E889U5RNN, 789U1901C5, QR44N9XPJQ, 1MBW07J51Q, BQN1B9B9HA, 1PIP394IIDUPC 0366096115050
Pharmacologic class: Copper-containing Intrauterine Device

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

N466096011505 followed by a unit qualifier and the quantity

Package 66096-0115-05. 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. **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)