NDC 43406-0124

CENTROCODE

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.

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 ID43406-0124_3d257ccd-5bd0-462c-a9b3-76b7224f484e
NDC43406-0124
Product TypeHuman Otc Drug
Proprietary NameCENTROCODE
Generic NameAmerican 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 FormLiquid
Route of AdministrationORAL
Marketing Start Date2010-01-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameNatural Creations, Inc.
Substance NameAMERICAN 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 Strength3 [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 FlagN
Listing Certified Through2022-12-31

Packaging

NDC 43406-0124-1

30 mL in 1 BOTTLE, DROPPER (43406-0124-1)
Marketing Start Date2010-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 43406-0124-1 [43406012401]

CENTROCODE LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-01-01

Drug Details


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