NDC 48951-1098

Argentum Quartz

Argentum Quartz

Argentum Quartz is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc.. The primary component is Silver; Silicon Dioxide.

• Product ID: 48951-1098_69fcd5ab-ab8c-9e64-e053-2991aa0a44be
• NDC: 48951-1098
• Product Type: Human Otc Drug
• Proprietary Name: Argentum Quartz
• Generic Name: Argentum 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: SILVER; SILICON DIOXIDE
• Active Ingredient Strength: 20 [hp_X]/mL; [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 48951-1098-1

10 AMPULE in 1 BOX (48951-1098-1) > 1 mL in 1 AMPULE

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

NDC SPL Data Element Entries

NDC 48951-1098-1 [48951109801]

Argentum Quartz LIQUID

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

Drug Details

Active Ingredients

Ingredient	Strength
SILVER	20 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 765c8c8f-0727-45da-a77e-c3907a3d0793
• Manufacturer:
  • Uriel Pharmacy Inc.
• UNII:
  • ETJ7Z6XBU4
  • 3M4G523W1G

NDC Crossover Matching brand name "Argentum Quartz" or generic name "Argentum Quartz"

NDC	Brand Name	Generic Name
48951-1097	Argentum Quartz	Argentum Quartz
48951-1098	Argentum Quartz	Argentum Quartz
53645-1340	Argentum Quartz	Argentum Quartz