NDC 43742-0838

Salsolinol

Salsolinol

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

• Product ID: 43742-0838_9e7f2b77-a24f-4d03-b8b9-fce5be8d387c
• NDC: 43742-0838
• Product Type: Human Otc Drug
• Proprietary Name: Salsolinol
• Generic Name: Salsolinol
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2016-08-24
• 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
• Listing Certified Through: 2020-12-31

Packaging

NDC 43742-0838-1

30 mL in 1 BOTTLE, DROPPER (43742-0838-1)

• Marketing Start Date: 2016-08-24
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43742-0838-1 [43742083801]

Salsolinol LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-08-24

Drug Details

Active Ingredients

Ingredient	Strength
SALSOLINOL	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: f33c9592-fcd8-44af-a49f-94d13304f725
• 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