Ohm Cholesterol Aid NDC 66096-191

NDC codes

FDA NDC Directory

Product NDC (as listed)66096-191Labeler and product segments. Claims need a package NDC.

Product NDC at billing width66096-0191Add 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
66096-191-05	66096019105	59 mL in 1 BOTTLE, SPRAY (66096-191-05)Marketed from Jan 10, 2017

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): Ohm Cholesterol Aid
Generic name (nonproprietary): cholesterinum, fel tauri, guatteria guameri.
Active ingredients: Cholesterol — 13 [hp_C]/59mLBos taurus bile — 3 [hp_X]/59mLMalmea depressa bark — 5 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: OHM PHARMA INC.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 10, 2017
Listing expires: Dec 31, 2026
Identifiers: Product ID 66096-191_d44ad1d9-cfb0-62c1-e053-2a95a90a323eSPL ID d44ad1d9-cfb0-62c1-e053-2a95a90a323eSPL set ID 21fea9e1-4f35-4044-b0e2-645961906b7dUNII 97C5T2UQ7J, ET3651ZLOU, XA09475C3BUPC 0366096191054

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

N466096019105 followed by a unit qualifier and the quantity

Package 66096-0191-05. 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 ailments related with slow hepatic metabolism resulting in elevated cholesterol levels.** **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)