NDC 43742-0394

PHLORIDZIN

Phloridzinum

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

• Product ID: 43742-0394_732d1217-3638-4b6f-9db1-5ba26e86f0a3
• NDC: 43742-0394
• Product Type: Human Otc Drug
• Proprietary Name: PHLORIDZIN
• Generic Name: Phloridzinum
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2014-09-29
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Deseret Biologicals, Inc.
• Substance Name: PHLORIZIN
• Active Ingredient Strength: 6 [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 43742-0394-1

30 mL in 1 BOTTLE, DROPPER (43742-0394-1)

• Marketing Start Date: 2016-07-28
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43742-0394-1 [43742039401]

PHLORIDZIN LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-07-28

Drug Details

Active Ingredients

Ingredient	Strength
PHLORIZIN	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 65c70a7c-175f-4f76-bd97-bb691897997c
• Manufacturer:
  • Deseret Biologicals, Inc.
• UNII:
  • CU9S17279X

NDC Crossover Matching brand name "PHLORIDZIN" or generic name "Phloridzinum"

NDC	Brand Name	Generic Name
43742-0394	PHLORIDZIN	Phloridzinum
43857-0347	PHLORIDZIN	NOT APPLICABLE
63083-1535	Phloridzin	Phloridzin
44911-0372	Phloridzin Phenolic	Phloridzinum
44911-0509	Phloridzin Phenolic	Phloridzinum