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NDC 43742-2126-01 Progenite 20; 6; 6; 6; 6; 12; 12; 6; 12; 12; 6; 6; 12; 12; 6; 6; 6; 6; 8; 6; 8 [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 Details
Progenite 20; 6; 6; 6; 6; 12; 12; 6; 12; 12; 6; 6; 12; 12; 6; 6; 6; 6; 8; 6; 8 [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
Progenite is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by Deseret Biologicals. The primary component is ALCOHOL, X-RAY EXPOSED (1000 RAD); ALLYLTHIOUREA; AMMONIUM CARBONATE; BARIUM CHLORIDE DIHYDRATE; CAULOPHYLLUM THALICTROIDES ROOT; CHASTE TREE FRUIT; CONIUM MACULATUM FLOWERING TOP; ESTRONE; GRAPHITE; HYOSCYAMUS NIGER; JUNIPERUS SABINA LEAFY TWIG; SAW PALM.
Product Information
| NDC | 43742-2126 |
|---|---|
| Product ID | 43742-2126_e30cdb3e-749d-4b0b-8c89-d74c24671c3f |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Progenite |
| Proprietary Name Suffix | n/a |
| 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, C |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | LIQUID |
| Route | ORAL |
| Active Ingredient Strength | 20; 6; 6; 6; 6; 12; 12; 6; 12; 12; 6; 6; 12; 12; 6; 6; 6; 6; 8; 6; 8 |
| Active Ingredient Units | [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 |
| Substance Name | ALCOHOL, X-RAY EXPOSED (1000 RAD); ALLYLTHIOUREA; AMMONIUM CARBONATE; BARIUM CHLORIDE DIHYDRATE; CAULOPHYLLUM THALICTROIDES ROOT; CHASTE TREE FRUIT; CONIUM MACULATUM FLOWERING TOP; ESTRONE; GRAPHITE; HYOSCYAMUS NIGER; JUNIPERUS SABINA LEAFY TWIG; SAW PALM |
| Labeler Name | Deseret Biologicals |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | UNAPPROVED HOMEOPATHIC |
| Application Number | n/a |
| Listing Certified Through | 2024-12-31 |
Package
NDC 43742-2126-01 (43742212601)
| NDC Package Code | 43742-2126-1 |
|---|---|
| Billing NDC | 43742212601 |
| Package | 30 mL in 1 BOTTLE, DROPPER (43742-2126-1) |
| Marketing Start Date | 2023-12-21 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |