Progenite NDC 43742-2126

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-2126Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-2126Add 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
43742-2126-1	43742212601	30 mL in 1 BOTTLE, DROPPER (43742-2126-1)Marketed from Dec 21, 2023

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): Progenite
Generic name (nonproprietary): ammonium carbonicum, baryta muriatica, borax, caulophyllum thalictroides, natrum carbonicum, sabal serrulata, sabina, sulphuricum acidum, thiosinaminum, folliculinum, tuba uterina suis, uterus suis, hypothalamus (suis), thyroidinum (suis), agnus castus, conium maculatum, graphites, hyoscyamus niger, sepia, selenium metallicum, x-ray
Active ingredients: Ammonium carbonate — 6 [hp_X]/mLBarium chloride dihydrate — 6 [hp_X]/mLSodium borate — 6 [hp_X]/mLCaulophyllum thalictroides root — 6 [hp_X]/mLSodium carbonate — 6 [hp_X]/mLSaw palmetto — 6 [hp_X]/mLJuniperus sabina leafy twig — 6 [hp_X]/mLSulfuric acid — 6 [hp_X]/mLAllylthiourea — 6 [hp_X]/mLEstrone — 6 [hp_X]/mLSus scrofa fallopian tube — 6 [hp_X]/mLSus scrofa uterus — 6 [hp_X]/mLSus scrofa hypothalamus — 8 [hp_X]/mLThyroid — 8 [hp_X]/mLChaste tree fruit — 12 [hp_X]/mLConium maculatum flowering top — 12 [hp_X]/mLGraphite — 12 [hp_X]/mLHyoscyamus niger — 12 [hp_X]/mLSepia officinalis juice — 12 [hp_X]/mLSelenium — 12 [hp_X]/mLAlcohol, X-ray exposed (1000 rad) — 20 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 21, 2023
Listing expires: Dec 31, 2026
Identifiers: Product ID 43742-2126_2304d23a-ad78-47c7-bb28-8c02012cc1d9SPL ID 2304d23a-ad78-47c7-bb28-8c02012cc1d9SPL set ID dfc114e0-34d4-4ae4-bba8-a8a1b7ad6a24UNII NJ5VT0FKLJ, EL5GJ3U77E, 91MBZ8H3QO, JTJ6HH6YEH, 45P3261C7T, J7WWH9M8QS, Z5BEX9K2G1, O40UQP6WCF, 706IDJ14B7, 2DI9HA706A, 2HA12BTZ65, 2595C75F1P, N6R0856Z79, 6RV024OAUQ, 433OSF3U8A, Q28R5GF371, 4QQN74LH4O, 4WRK2153H3, QDL83WN8C2, H6241UJ22B, 6PRJ93602PUPC 0810151882307

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

N443742212601 followed by a unit qualifier and the quantity

Package 43742-2126-01. 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 Oct 23, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • fertility support • irregular menses • hormonal support • reduced sex drive 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)