- Product NDC
- 43772-0018
- 11-digit product format
- 437720018
- Labeler code
- 43772
- Product ID
- 43772-0018_0cd11851-8428-45e4-8a32-a26b8f67596a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cholinum, Inositol, Lithium Carbonicum, Pulsatilla, Ignatia Amara, GABA, Pituitaria Glandula (Suis), Pineal (Suis), Dopamine, Serotonin
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Synergy Formulas, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2013-08-22
- Marketing end
- 0000-00-00
- Substance
- CHOLINE HYDROXIDE; INOSITOL; LITHIUM CARBONATE; PULSATILLA VULGARIS; STRYCHNOS IGNATII SEED; .GAMMA.-AMINOBUTYRIC ACID; SUS SCROFA PITUITARY GLAND; SUS SCROFA PINEAL GLAND; DOPAMINE; SEROTONIN; GOLD; SODIUM CHLORIDE; PETROSELINUM CRISPUM; SULFUR
- Active 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_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- Pharmacologic classes
- Mood Stabilizer [EPC],Catecholamine [EPC],Catecholamines [CS],Standardized Chemical Allergen [EPC],Increased Histamine Release [PE],Allergens [CS],Cell-mediated Immunity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record