NDC 43742-0883

Borrelia Babesia Kit

Babesia Microti, Borrelia Burgdorferi Nosode

Borrelia Babesia Kit is a Kit in the Human Otc Drug category. It is labeled and distributed by Deseret Biologicals, Inc.. The primary component is .

• Product ID: 43742-0883_6bd6eafa-d383-42ab-b8c1-6f97d98a944b
• NDC: 43742-0883
• Product Type: Human Otc Drug
• Proprietary Name: Borrelia Babesia Kit
• Generic Name: Babesia Microti, Borrelia Burgdorferi Nosode
• Dosage Form: Kit
• Marketing Start Date: 2016-10-27
• Marketing End Date: 2022-10-24
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Deseret Biologicals, Inc.
• Active Ingredient Strength: 0
• NDC Exclude Flag: N

Packaging

NDC 43742-0883-1

1 DOSE PACK in 1 CARTON (43742-0883-1) > 1 KIT in 1 DOSE PACK * 2 mL in 1 VIAL, SINGLE-DOSE (43742-0888-1) * 2 mL in 1 VIAL, SINGLE-DOSE (43742-0892-1) * 2 mL in 1 VIAL, SINGLE-DOSE (43742-0891-1) * 2 mL in 1 VIAL, SINGLE-DOSE (43742-0890-1) * 2 mL in 1 VIAL, SINGLE-DOSE (43742-0889-1) * 2 mL in 1 VIAL, SINGLE-DOSE (43742-0893-1) * 2

• Marketing Start Date: 2016-10-27
• Marketing End Date: 2022-10-24
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43742-0883-1 [43742088301]

Borrelia Babesia Kit KIT

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-10-27

Drug Details

OpenFDA Data

• SPL SET ID: af884772-564e-4fab-9fef-37557c417053
• Manufacturer:
  • Deseret Biologicals, Inc.

NDC Crossover Matching brand name "Borrelia Babesia Kit" or generic name "Babesia Microti, Borrelia Burgdorferi Nosode"

NDC	Brand Name	Generic Name
43742-0883	Borrelia Babesia Kit	Babesia Microti, Borrelia Burgdorferi Nosode
43742-1716	BOBA HOMO	Babesia Microti, Borrelia Burgdorferi Nosode
43742-0246	Borrelia Babesia Remedy	Babesia Microti, Borrelia Burgdorferi Nosode
43742-0654	Borrelia Babesia Remedy	Babesia Microti, Borrelia Burgdorferi Nosode
43742-0854	Borrelia-Babesia Homochord	Babesia Microti, Borrelia Burgdorferi Nosode