Progenite NDC 43742-1170

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1170Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1170Add 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
43742-1170-1	43742117001	30 mL in 1 BOTTLE, DROPPER (43742-1170-1)Marketed from Feb 19, 2018

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 — 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) — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 19, 2018
Marketing end: Jun 1, 2028
Identifiers: Product ID 43742-1170_c1ecefa2-d637-4d59-a749-4bc66d88fc27SPL ID c1ecefa2-d637-4d59-a749-4bc66d88fc27SPL set ID 6051c9d5-36ef-4bfa-baab-9862c94805fbUNII NJ5VT0FKLJ, EL5GJ3U77E, 91MBZ8H3QO, JTJ6HH6YEH, 45P3261C7T, J7WWH9M8QS, Z5BEX9K2G1, O40UQP6WCF, 706IDJ14B7, 2DI9HA706A, 2HA12BTZ65, 2595C75F1P, N6R0856Z79, 6RV024OAUQ, 433OSF3U8A, Q28R5GF371, 4QQN74LH4O, 4WRK2153H3, QDL83WN8C2, H6241UJ22B, 6PRJ93602P

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

N443742117001 followed by a unit qualifier and the quantity

Package 43742-1170-01. 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 Dec 12, 2023.

Indications (excerpt from the label)

HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to impaired reproductive activity in both males and females, such as hormonal imbalances, reduced sex drive, and irregular menses.** **These statements are based upon traditional 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)