What is NDC 43742-1935?

43742-1935 is the product NDC for Myco Homo (mycoplasma pneumoniae), Mycoplasma pneumoniae 15 [hp_X]/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?

Myco Homo (Mycoplasma Pneumoniae).

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 Myco 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.

Myco Homo NDC 43742-1935 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1935Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1935Add 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
43742-1935-1	4374219350143742193501	30 mL in 1 BOTTLE, DROPPER (43742-1935-1)Marketed from Apr 20, 2021

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): Myco Homo
Generic name (nonproprietary): mycoplasma pneumoniae
Active ingredients: Mycoplasma pneumoniae — 15 [hp_X]/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: Apr 20, 2021
Listing expires: Dec 31, 2026
Identifiers: Product ID 43742-1935_2cb80b5f-80f2-4a24-84dc-fdc1333f2bf8SPL ID 2cb80b5f-80f2-4a24-84dc-fdc1333f2bf8SPL set ID ce805acf-db0b-4b1f-ab3e-36bcb8cc1e57UNII JQE470FAD0UPC 0810151883144

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

N443742193501 followed by a unit qualifier and the quantity

Package 43742-1935-01. 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 19, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • head pain • muscle pain • joint pain • nausea 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 43742-1935

What is NDC 43742-1935?: 43742-1935 is the product NDC for Myco Homo (mycoplasma pneumoniae), Mycoplasma pneumoniae 15 [hp_X]/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?: Myco Homo (Mycoplasma Pneumoniae).
What is the active ingredient?: Mycoplasma pneumoniae.
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 Myco 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.

Myco Homo (Mycoplasma pneumoniae) NDC 43742-1935