CENTROCODE is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Natural Creations, Inc.. The primary component is American Ginseng; Adenosine Triphosphate; Corticotropin; Alfalfa; Bos Taurus Hypothalamus; Phytolacca Americana Root; Bos Taurus Pituitary Gland, Posterior; Thyroid, Unspecified; Iodine; Silicon Dioxide; Oyster Shell Calcium Carbonate, Crude; Strychnos Ignatii Seed; Iridium; Lachesis Muta Venom; Lycopodium Clavatum Spore; Sodium Chloride; Strychnos Nux-vomica Seed; Phosphorus; Selenium; Uranyl Nitrate Hexahydrate.
Product ID | 43406-0124_3d257ccd-5bd0-462c-a9b3-76b7224f484e |
NDC | 43406-0124 |
Product Type | Human Otc Drug |
Proprietary Name | CENTROCODE |
Generic Name | American Ginseng, Adenosine Triphosphate, Corticotropin, Alfalfa, Bos Taurus Hypothalamus, Phytolacca Americana Root, Bos Taurus Pituitary Gland Posterior, Thyroid Unspecified, Iodine, Silicon Dioxide, Oster Shell Calcium Carbonate Crude, Strychnos Ignatii Seed, Iridium, Lachesis Muta Venom, Lycopodium Clavatum Spore, Sodium Chloride, Strychnos Nux-vomica Seed, Phosphorus, Selenium, Uranyl Nitrate Hexahydrate. |
Dosage Form | Liquid |
Route of Administration | ORAL |
Marketing Start Date | 2010-01-01 |
Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
Labeler Name | Natural Creations, Inc. |
Substance Name | AMERICAN GINSENG; ADENOSINE TRIPHOSPHATE; CORTICOTROPIN; ALFALFA; BOS TAURUS HYPOTHALAMUS; PHYTOLACCA AMERICANA ROOT; BOS TAURUS PITUITARY GLAND, POSTERIOR; THYROID, UNSPECIFIED; IODINE; SILICON DIOXIDE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; STRYCHNOS IGNATII SEED; IRIDIUM; LACHESIS MUTA VENOM; LYCOPODIUM CLAVATUM SPORE; SODIUM CHLORIDE; STRYCHNOS NUX-VOMICA SEED; PHOSPHORUS; SELENIUM; URANYL NITRATE HEXAHYDRATE |
Active Ingredient Strength | 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [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 |
NDC Exclude Flag | N |
Listing Certified Through | 2022-12-31 |
Marketing Start Date | 2010-01-01 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-01-01 |
Ingredient | Strength |
---|---|
AMERICAN GINSENG | 3 [hp_X]/mL |
SPL SET ID: | e5bbe9ec-7602-4de5-907a-7047c10198b6 |
Manufacturer | |
UNII | |
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