Coxs Homo NDC 43742-1794

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1794Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1794Add 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
43742-1794-1	43742179401	30 mL in 1 BOTTLE, DROPPER (43742-1794-1)Marketed from Sep 23, 2020

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): Coxs Homo
Generic name (nonproprietary): coxsackie nosode a2, coxsackie nosode b1, coxsackie nosode b3, coxsackie nosode b4, coxsackie nosode a7
Active ingredients: Human coxsackievirus a2 — 15 [hp_C]/mLHuman coxsackievirus b1 — 15 [hp_C]/mLHuman coxsackievirus b3 — 15 [hp_C]/mLHuman coxsackievirus b4 — 30 [hp_C]/mLHuman coxsackievirus a7 — 45 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 23, 2020
Listing expires: Dec 31, 2026
Identifiers: Product ID 43742-1794_c078614a-40a7-43dc-bfa8-9b23d4fd4268SPL ID c078614a-40a7-43dc-bfa8-9b23d4fd4268SPL set ID cd07aa76-d632-45fc-a323-d4ebf31beaf5UNII 82KK5J435E, ADL68M27WD, 69O1DAO10G, FYF75V7FDY, P3026TK92OUPC 0810151882727

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

N443742179401 followed by a unit qualifier and the quantity

Package 43742-1794-01. 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 Mar 19, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • fatigue • joint pain • headache These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)