Bart Homo NDC 43742-1700

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1700Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1700Add 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
43742-1700-1	43742170001	30 mL in 1 BOTTLE, DROPPER (43742-1700-1)Marketed from Sep 28, 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): Bart Homo
Generic name (nonproprietary): bartonella bacilliformis, bartonella clarridgeiae, bartonella elizabethae, bartonella henselae, bartonella quintana, bartonella vinsonii, bartonella washoensis
Active ingredients: Bartonella bacilliformis — 15 [hp_X]/mLBartonella clarridgeiae — 15 [hp_X]/mLBartonella elizabethae — 15 [hp_X]/mLBartonella henselae — 15 [hp_X]/mLBartonella quintana — 15 [hp_X]/mLBartonella vinsonii — 15 [hp_X]/mLBartonella washoensis — 15 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 28, 2020
Marketing end: Dec 12, 2028
Identifiers: Product ID 43742-1700_e4770c5a-3627-4793-be16-bcb6b9c859c2SPL ID e4770c5a-3627-4793-be16-bcb6b9c859c2SPL set ID b602cc5b-20eb-4f25-861f-46adaedf5a12UNII FHE1Q0VN6P, OZ0ND08BLR, 437GVI6AH4, 84PG7W9845, 9R2271TA4J, NF30MCQ9AC, 4040O0IM00

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

N443742170001 followed by a unit qualifier and the quantity

Package 43742-1700-01. 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 Feb 13, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • fever • head pain • chills • back pain • malaise 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)