Candida HP is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Natural Creations, Inc.. The primary component is Echinacea Purpurea; Baptisia Tinctoria Root; Glycyrrhiza Glabra; Astragalus Nuttallii Leaf; Sodium Borate; Oyster Shell Calcium Carbonate, Crude; Wood Creosote; Lycopodium Clavatum Spore; Sodium Phosphate, Dibasic, Heptahydrate; Nitric Acid; Strychnos Nux-vomica Seed; Phosphoric Acid; Pulsatilla Vulgaris; Sepia Officinalis Juice; Thuja Occidentalis Leafy Twig; Candida Albicans; Candida Albicans; Candida Albicans.
| Product ID | 43406-0011_44f82d12-c64b-4df9-889b-dc87f5883baf |
| NDC | 43406-0011 |
| Product Type | Human Otc Drug |
| Proprietary Name | Candida HP |
| Generic Name | Echinacea Purpurea, Baptisia Tinctoria Root, Glycyrrhiza Glabra, Astragalus Nuttallii Leaf, Sodium Borate, Oyster Shell Calcium Carbonate, Crude, Wood Creosote, Lycopodium Clavatum Spore, Sodium Phosphate, Dibasic Heptahydrate, Nitric Acid, Strychnos Nux-vomica Seed, Phosphoric Acid, Pulsatilla Vulgaris, Sepia Officinalis Juice, Candida Albicans |
| Dosage Form | Liquid |
| Route of Administration | ORAL |
| Marketing Start Date | 2007-05-29 |
| Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
| Labeler Name | Natural Creations, Inc. |
| Substance Name | ECHINACEA PURPUREA; BAPTISIA TINCTORIA ROOT; GLYCYRRHIZA GLABRA; ASTRAGALUS NUTTALLII LEAF; SODIUM BORATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; WOOD CREOSOTE; LYCOPODIUM CLAVATUM SPORE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; NITRIC ACID; STRYCHNOS NUX-VOMICA SEED; PHOSPHORIC ACID; PULSATILLA VULGARIS; SEPIA OFFICINALIS JUICE; THUJA OCCIDENTALIS LEAFY TWIG; CANDIDA ALBICANS; CANDIDA ALBICANS; CANDIDA ALBICANS |
| Active Ingredient Strength | 1 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
| Marketing Start Date | 2007-05-29 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2007-05-29 |
| Inactivation Date | 2019-11-27 |
| Ingredient | Strength |
|---|---|
| ECHINACEA PURPUREA | 1 [hp_X]/mL |
| SPL SET ID: | a6951cde-7c8e-4cc6-ae98-c3b6f66b90d1 |
| Manufacturer | |
| UNII | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 43406-0011 | Candida HP | Echinacea Purpurea, Baptisia Tinctoria Root, Glycyrrhiza Glabra, Astragalus Nuttallii Leaf, Sodium Borate, Oyster Shell Calcium Carbonate, Crude, Wood Creosote, Lycopodium Clavatum Spore, Sodium Phosphate, Dibasic Heptahydrate, Nitric Acid, Strychnos Nux-Vomica Seed, Phosphoric Acid, Pulsatilla Vulgaris, Sepia Officinalis Juice, Candida Albicans |
| 43406-0672 | Candida HP | Baptisia Tinctoria Root, Echinacea Purpurea, Glycyrrhiza Glabra, Astragalus Nuttallii Leaf, Candida Albicans, Sodium Borate, Oyster Shell Calcium Carbonate, Crude, Wood Creosote, Lycopodium Clavatum Spore, Strychnos Nux-Vomica Seed, Phosphoric Acid, Anemone Pulsatilla, Sepia Officinalis Juice, Thuja Occidentalis Leafy Twig, Sodium Phosphate, Dibasic, Heptahydrate, Nitric Acid |