| Product ID | 63083-2120_26a2a809-a305-48c7-b739-6efd1eff9cee |
| NDC | 63083-2120 |
| Product Type | Human Otc Drug |
| Proprietary Name | Teething Drops 2120 |
| Generic Name | Teething Drops |
| Dosage Form | Liquid |
| Route of Administration | ORAL |
| Marketing Start Date | 1984-08-15 |
| Marketing Category | UNAPPROVED HOMEOPATHIC / |
| Labeler Name | Professional Complementary Health Formulas |
| Substance Name | ARTEMISIA ANNUA FLOWERING TOP; BRYONIA ALBA ROOT; CITRULLUS COLOCYNTHIS FRUIT PULP; CLEMATIS RECTA FLOWERING TOP; COPPER; EUGENOL; MENTHA X PIPERITA WHOLE; MYRRH; OYSTER SHELL CALCIUM CARBONATE, CRUDE; ULMUS RUBRA BARK |
| Active Ingredient Strength | 3 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL |
| Pharm Classes | Allergens [CS], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Increased Histamine Release [PE], Inhibit Ovum Fertilization [PE], Standardized Chemical Allergen [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |