"43742-1170-1" National Drug Code (NDC)

NDC Code	43742-1170-1
Package Description	30 mL in 1 BOTTLE, DROPPER (43742-1170-1)
Product NDC	43742-1170
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Progenite
Non-Proprietary Name	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
Dosage Form	LIQUID
Usage	ORAL
Start Marketing Date	20180219
End Marketing Date	20280601
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	Deseret Biologicals
Substance Name	ALCOHOL, X-RAY EXPOSED (1000 RAD); ALLYLTHIOUREA; AMMONIUM CARBONATE; BARIUM CHLORIDE DIHYDRATE; CAULOPHYLLUM THALICTROIDES ROOT; CHASTE TREE; CONIUM MACULATUM FLOWERING TOP; ESTRONE; GRAPHITE; HYOSCYAMUS NIGER; JUNIPERUS SABINA LEAFY TWIG; SAW PALMETTO; SELENIUM; SEPIA OFFICINALIS JUICE; SODIUM BORATE; SODIUM CARBONATE; SULFURIC ACID; SUS SCROFA FALLOPIAN TUBE; SUS SCROFA HYPOTHALAMUS; SUS SCROFA UTERUS; THYROID
Strength	12; 6; 6; 6; 6; 12; 12; 6; 12; 12; 6; 6; 12; 12; 6; 6; 6; 6; 8; 6; 8
Strength Unit	[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL