NDC 48951-2054

Berberis Quartz

Berberis Quartz

Berberis Quartz is a Oral Liquid 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: 48951-2054_6cb7e1f8-ecf5-df39-e053-2a91aa0ac352
• NDC: 48951-2054
• Product Type: Human Otc Drug
• Proprietary Name: Berberis Quartz
• Generic Name: Berberis Quartz
• Dosage Form: Liquid
• 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]/mL; [hp_X]/mL; [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 48951-2054-1

10 AMPULE in 1 BOX (48951-2054-1) > 1 mL in 1 AMPULE

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

NDC SPL Data Element Entries

NDC 48951-2054-1 [48951205401]

Berberis Quartz LIQUID

• 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]/mL

OpenFDA Data

• SPL SET ID: 5da48d70-1140-495d-b672-0e55c04196e1
• 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