NDC 43742-0303

Salsolinol

Salsolinol

Salsolinol is a Oral Liquid in the Human Prescription Drug category. It is labeled and distributed by Deseret Biologicals, Inc.. The primary component is Salsolinol.

• Product ID: 43742-0303_2f38346d-5b60-4f35-a6a2-f646a9f12b89
• NDC: 43742-0303
• Product Type: Human Prescription Drug
• Proprietary Name: Salsolinol
• Generic Name: Salsolinol
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2014-01-09
• Marketing End Date: 2019-12-29
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Deseret Biologicals, Inc.
• Substance Name: SALSOLINOL
• Active Ingredient Strength: 6 [hp_X]/mL
• NDC Exclude Flag: N

Packaging

NDC 43742-0303-1

30 mL in 1 BOTTLE, DROPPER (43742-0303-1)

• Marketing Start Date: 2014-01-09
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43742-0303-1 [43742030301]

Salsolinol LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2014-01-09
• Marketing End Date: 2019-12-29

Drug Details

Active Ingredients

Ingredient	Strength
SALSOLINOL	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: f67bb80b-9eaf-45e4-9f3c-10fcd692b6f7
• Manufacturer:
  • Deseret Biologicals, Inc.
• UNII:
  • 9ILS801M65

NDC Crossover Matching brand name "Salsolinol" or generic name "Salsolinol"

NDC	Brand Name	Generic Name
43742-0303	Salsolinol	Salsolinol
43742-0663	Salsolinol	Salsolinol
43742-0838	Salsolinol	Salsolinol
43857-0365	Salsolinol	Salsolinol
43857-0501	Salsolinol	Salsolinol (Hydrochloride)
63083-1542	Salsolinol	Salsolinol