NDC 48951-1203

Aurum Prunus

Aurum Prunus

Aurum Prunus is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc.. The primary component is Sloe; Gold.

• Product ID: 48951-1203_6a10217e-c0c4-4f4c-e053-2991aa0a3fcd
• NDC: 48951-1203
• Product Type: Human Otc Drug
• Proprietary Name: Aurum Prunus
• Generic Name: Aurum Prunus
• 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: SLOE; GOLD
• Active Ingredient Strength: 6 [hp_X]/mL; [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 48951-1203-3

60 mL in 1 BOTTLE, DROPPER (48951-1203-3)

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

NDC SPL Data Element Entries

NDC 48951-1203-3 [48951120303]

Aurum Prunus LIQUID

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

Drug Details

Active Ingredients

Ingredient	Strength
SLOE	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 31918b12-fa91-48bc-a420-71c668042b3c
• Manufacturer:
  • Uriel Pharmacy Inc.
• UNII:
  • 3MLB4858X7
  • 79Y1949PYO

NDC Crossover Matching brand name "Aurum Prunus" or generic name "Aurum Prunus"

NDC	Brand Name	Generic Name
48951-1202	Aurum Prunus	Aurum Prunus
48951-1203	Aurum Prunus	Aurum Prunus
48951-1204	Aurum Prunus	Aurum Prunus