| Product ID | 63083-2089_9f8c3fdd-a177-449d-b9b2-1aad83b02c4a |
| NDC | 63083-2089 |
| Product Type | Human Otc Drug |
| Proprietary Name | Pain Formula I Drops 2089 |
| Generic Name | Pain Formula I 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 | ACONITUM NAPELLUS WHOLE; AMARYLLIS BELLADONNA WHOLE; BRYONIA ALBA ROOT; COFFEA ARABICA SEED, ROASTED; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; SPIGELIA MARILANDICA ROOT |
| Active Ingredient Strength | 5 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL |
| Pharm Classes | Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |