NDC 48951-2055

BERBERIS QUARTZ

Berberis Quartz

BERBERIS QUARTZ is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc.. The primary component is Berberis Vulgaris Root Bark; Bos Taurus Nasal Mucosa; Silicon Dioxide.

• Product ID: 48951-2055_6d94f4d0-0a6d-b284-e053-2a91aa0ab707
• NDC: 48951-2055
• Product Type: Human Otc Drug
• Proprietary Name: BERBERIS QUARTZ
• Generic Name: Berberis Quartz
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 2009-09-01
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: URIEL PHARMACY INC.
• Substance Name: BERBERIS VULGARIS ROOT BARK; BOS TAURUS NASAL MUCOSA; SILICON DIOXIDE
• Active Ingredient Strength: 3 [hp_X]/1; [hp_X]/1; [hp_X]/1
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 48951-2055-2

1350 PELLET in 1 BOTTLE, GLASS (48951-2055-2)

• Marketing Start Date: 2009-09-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 48951-2055-2 [48951205502]

BERBERIS QUARTZ PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2009-09-01

Drug Details

Active Ingredients

Ingredient	Strength
BERBERIS VULGARIS ROOT BARK	3 [hp_X]/1

OpenFDA Data

• SPL SET ID: 0102455e-918c-4f68-a04f-8d2d3948bc2c
• Manufacturer:
  • URIEL PHARMACY INC.
• UNII:
  • 1TH8Q20J0U
  • ETJ7Z6XBU4
  • 343455G79K

NDC Crossover Matching brand name "BERBERIS QUARTZ" or generic name "Berberis Quartz"

NDC	Brand Name	Generic Name
48951-2054	Berberis Quartz	Berberis Quartz
48951-2055	BERBERIS QUARTZ	BERBERIS QUARTZ