| Product ID | 63083-3012_b177d085-8f6b-405e-aced-ef10f26b834d |
| NDC | 63083-3012 |
| Product Type | Human Otc Drug |
| Proprietary Name | Oxy Bee Pollen Liquescence 3012 |
| Generic Name | Oxy Bee Pollen Liquescence |
| 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 | BEE POLLEN; BITTER ALMOND; COMFREY ROOT; DNA-DIRECTED RNA POLYMERASE SUBUNIT BETA (M. TUBERCULOSIS); ENGLISH SOLE; FUCUS VESICULOSUS; LAMINARIA JAPONICA; MEDICAGO SATIVA WHOLE; PANTOTHENIC ACID; ROYAL JELLY; ZINC |
| Active Ingredient Strength | 2 [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL |
| Pharm Classes | Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Fish Proteins, Dietary [EXT], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |