| NDC Code | 63083-2120-2 |
| Package Description | 59 mL in 1 BOTTLE, DROPPER (63083-2120-2) |
| Product NDC | 63083-2120 |
| Product Type Name | HUMAN OTC DRUG |
| Proprietary Name | Teething Drops |
| Proprietary Name Suffix | 2120 |
| Non-Proprietary Name | Teething Drops |
| Dosage Form | LIQUID |
| Usage | ORAL |
| Start Marketing Date | 19840815 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Manufacturer | 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 |
| Strength | 3; 12; 6; 6; 6; 3; 4; 6; 12; 3 |
| Strength Unit | [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 |
| Pharmacy 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] |