What is NDC 43742-1972?

43742-1972 is the product NDC for RockHomo, Rickettsia prowazekii 10 [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?

RockHomo (Rickettsia Nosode (Rickettsia Prowazekii)).

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 RockHomo?

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.

RockHomo NDC 43742-1972 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1972Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1972Add 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
43742-1972-1	4374219720143742197201	30 mL in 1 BOTTLE, DROPPER (43742-1972-1)Marketed from Sep 17, 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): RockHomo
Generic name (nonproprietary): rickettsia nosode (rickettsia prowazekii)
Active ingredients: Rickettsia prowazekii — 10 [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: Sep 17, 2020
Listing expires: Dec 31, 2026
Identifiers: Product ID 43742-1972_92ccb097-92a6-4189-b81d-6c26ad866b6eSPL ID 92ccb097-92a6-4189-b81d-6c26ad866b6eSPL set ID fefea641-ab32-48b6-87e3-39e20628228cUNII TVS414L9M5UPC 0810151883243

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

N443742197201 followed by a unit qualifier and the quantity

Package 43742-1972-01. 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 26, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • Rash • Fever • Nausea • Muscle Pain • Lack of Appetite • Abdominal Pain • Joint Pain • Occasional Diarrhea 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 43742-1972

What is NDC 43742-1972?: 43742-1972 is the product NDC for RockHomo, Rickettsia prowazekii 10 [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?: RockHomo (Rickettsia Nosode (Rickettsia Prowazekii)).
What is the active ingredient?: Rickettsia prowazekii.
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 RockHomo?: 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.