NDC 43742-0663

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: 43742-0663_bf5e72c6-4d54-4f46-8da4-e6657829cd4b
• NDC: 43742-0663
• Product Type: Human Otc Drug
• Proprietary Name: Salsolinol
• Generic Name: Salsolinol
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2015-11-16
• Marketing End Date: 2020-12-01
• 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 43742-0663-1

30 mL in 1 BOTTLE, DROPPER (43742-0663-1)

• Marketing Start Date: 2015-11-16
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43742-0663-1 [43742066301]

Salsolinol LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2015-11-16
• Marketing End Date: 2020-12-01

Drug Details

Active Ingredients

Ingredient	Strength
SALSOLINOL	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 1355c761-706c-4ac2-9c28-ca46e00f6f8f
• 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