What is NDC 43742-1729?

43742-1729 is the product NDC for Bruc Homo (brucella melitensis), Brucella melitensis 18 [hp_C]/mL liquid, listed with the FDA by Deseret Biologicals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Bruc Homo (Brucella Melitensis).

Deseret Biologicals, Inc., NDC labeler code 43742. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Bruc Homo?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Bruc Homo NDC 43742-1729 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1729Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1729Add 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
43742-1729-1	4374217290143742172901	30 mL in 1 BOTTLE, DROPPER (43742-1729-1)Marketed from Oct 2, 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): Bruc Homo
Generic name (nonproprietary): brucella melitensis
Active ingredients: Brucella melitensis — 18 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.NDC labeler code 43742
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 2, 2020
Listing expires: Dec 31, 2026
Identifiers: Product ID 43742-1729_d09f61f8-b7f4-49be-bcb5-e2e5353beb80SPL ID d09f61f8-b7f4-49be-bcb5-e2e5353beb80SPL set ID 916e818d-3f85-4020-ae9b-755d348576beUNII OQF85710LZUPC 0810151882512

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

N443742172901 followed by a unit qualifier and the quantity

Package 43742-1729-01. 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 Apr 23, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • fever • sweats • malaise • headache • back pain • neck pain • malodorous sweat • gut inflammation 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)

About NDC 43742-1729

What is NDC 43742-1729?: 43742-1729 is the product NDC for Bruc Homo (brucella melitensis), Brucella melitensis 18 [hp_C]/mL liquid, listed with the FDA by Deseret Biologicals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Bruc Homo (Brucella Melitensis).
What is the active ingredient?: Brucella melitensis.
Who is the labeler?: Deseret Biologicals, Inc., NDC labeler code 43742. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Bruc Homo?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Bruc Homo (Brucella melitensis) NDC 43742-1729