NDC 44911-0372

Phloridzin Phenolic

Phloridzinum

Phloridzin Phenolic is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Energique, Inc.. The primary component is Phlorizin.

• Product ID: 44911-0372_9220172d-caa2-4e21-8e50-06c1af514dc8
• NDC: 44911-0372
• Product Type: Human Otc Drug
• Proprietary Name: Phloridzin Phenolic
• Generic Name: Phloridzinum
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2017-03-28
• Marketing End Date: 2022-10-25
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Energique, Inc.
• Substance Name: PHLORIZIN
• Active Ingredient Strength: 6 [hp_X]/mL
• NDC Exclude Flag: N

Packaging

NDC 44911-0372-1

30 mL in 1 BOTTLE, DROPPER (44911-0372-1)

• Marketing Start Date: 2017-03-28
• Marketing End Date: 2022-10-25
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 44911-0372-1 [44911037201]

Phloridzin Phenolic LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2017-03-28
• Marketing End Date: 2022-10-25

Drug Details

Active Ingredients

Ingredient	Strength
PHLORIZIN	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 8c44f3e5-92f2-4933-be8d-660a460d48e0
• Manufacturer:
  • Energique, Inc.
• UNII:
  • CU9S17279X

NDC Crossover Matching brand name "Phloridzin Phenolic" or generic name "Phloridzinum"

NDC	Brand Name	Generic Name
44911-0372	Phloridzin Phenolic	Phloridzinum
44911-0509	Phloridzin Phenolic	Phloridzinum
43742-0394	PHLORIDZIN	Phloridzinum