NDC 43772-0018

DepressionComposition

Cholinum, Inositol, Lithium Carbonicum, Pulsatilla, Ignatia Amara, Gaba, Pituitaria Glandula (suis), Pineal (suis), Dopamine, Serotonin

DepressionComposition is a Oral Liquid in the Human Prescription Drug category. It is labeled and distributed by Synergy Formulas, Inc.. The primary component is 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.

• Product ID: 43772-0018_0cd11851-8428-45e4-8a32-a26b8f67596a
• NDC: 43772-0018
• Product Type: Human Prescription Drug
• Proprietary Name: DepressionComposition
• Generic Name: Cholinum, Inositol, Lithium Carbonicum, Pulsatilla, Ignatia Amara, Gaba, Pituitaria Glandula (suis), Pineal (suis), Dopamine, Serotonin
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2013-08-22
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Synergy Formulas, Inc.
• Substance Name: 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 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_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
• Pharm 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: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 43772-0018-1

60 mL in 1 BOTTLE, DROPPER (43772-0018-1)

• Marketing Start Date: 2013-08-22
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43772-0018-1 [43772001801]

DepressionComposition LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2013-08-22
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
CHOLINE HYDROXIDE	3 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 4c9bbe4f-44ae-4f99-8371-a607d81cc8cd
• Manufacturer:
  • Synergy Formulas, Inc.
• UNII:
  • 2BMD2GNA4V
  • 4L6452S749
  • 70FD1KFU70
  • 79Y1949PYO
  • 2ACZ6IPC6I
  • 050QZ2EDK7
  • 333DO1RDJY
  • 7THJ3EG9SY
  • 451W47IQ8X
  • I76KB35JEV
  • VTD58H1Z2X
  • 1NM3M2487K
  • 1WZA4Y92EX
  • L0PFEMQ1DT

Pharmacological Class

• Mood Stabilizer [EPC]
• Catecholamine [EPC]
• Catecholamines [CS]
• Standardized Chemical Allergen [EPC]
• Increased Histamine Release [PE]
• Allergens [CS]
• Cell-mediated Immunity [PE]