- Product NDC
- 43406-0617
- 11-digit product format
- 434060617
- Labeler code
- 43406
- Product ID
- 43406-0617_3331bc2f-9327-4614-af72-73ebdc415de8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Epinephrine, Glutamic Acid, Mucuna Pruriens Seed, Niacinamide, Serotonin, Ubidecarenone, Corticotropin, Ascorbic Acid, Adenosine Triphosphate, Insulin Pork, Sus Scrofa Parathyroid Gland, Sus Scrofa Pituitary Gland, Thiamine Hydrochloride, Thyroid, Anhydrous Citric Acid, Herring Sperm DNA, Saccharomyces Cerevisiae RNA, Anacardium Occidentale Fruit, Arsenic Trioxide, Aspartic Acid, Barium Carbonate, Oyster Shell Calcium Carbonate Crude, Lycopodium Clavatum Spore, Anemone Pulsatilla, Datura Stramonium, Sulfur
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Natural Creations, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2016-06-01
- Marketing end
- 0000-00-00
- Substance
- EPINEPHRINE; GLUTAMIC ACID; MUCUNA PRURIENS SEED; NIACINAMIDE; SEROTONIN; UBIDECARENONE; CORTICOTROPIN; ASCORBIC ACID; ADENOSINE TRIPHOSPHATE; INSULIN PORK; SUS SCROFA PARATHYROID GLAND; SUS SCROFA PITUITARY GLAND; THIAMINE HYDROCHLORIDE; THYROID, UNSPECIFIED; ANHYDROUS CITRIC ACID; HERRING SPERM DNA; SACCHAROMYCES CEREVISIAE RNA; ANACARDIUM OCCIDENTALE FRUIT; ARSENIC TRIOXIDE; ASPARTIC ACID; BARIUM CARBONATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; LYCOPODIUM CLAVATUM SPORE; ANEMONE PULSATILLA; DATURA STRAMONIUM; SULFUR
- Active strength
- 30 [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/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; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
- Pharmacologic classes
- Adrenergic alpha-Agonists [MoA],Adrenergic beta-Agonists [MoA],alpha-Adrenergic Agonist [EPC],beta-Adrenergic Agonist [EPC],Catecholamine [EPC],Catecholamines [CS],Adrenocorticotropic Hormone [CS],Adrenocorticotropic Hormone [EPC],Vitamin C [EPC],Ascorbic Acid [CS],Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record