NDC 43742-0217

Quercetin

Quercetin

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

• Product ID: 43742-0217_cd703286-4402-499a-89c5-03390999d55a
• NDC: 43742-0217
• Product Type: Human Otc Drug
• Proprietary Name: Quercetin
• Generic Name: Quercetin
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2013-04-11
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Deseret Biologicals, Inc.
• Substance Name: QUERCETIN
• Active Ingredient Strength: 6 [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 43742-0217-1

30 mL in 1 BOTTLE, DROPPER (43742-0217-1)

• Marketing Start Date: 2013-04-11
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43742-0217-1 [43742021701]

Quercetin LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-04-11

Drug Details

Active Ingredients

Ingredient	Strength
QUERCETIN	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 87dec202-711c-4270-a176-306cf6365558
• Manufacturer:
  • Deseret Biologicals, Inc.
• UNII:
  • 9IKM0I5T1E

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

NDC	Brand Name	Generic Name
43742-0217	Quercetin	Quercetin
43857-0067	Quercetin	Quercetin
57520-1003	Quercetin	Quercetin,
63083-1540	Quercetin	Quercetin