NDC 48951-1318

Aurum 21X

Aurum 21x

Aurum 21X is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc.. The primary component is Gold.

• Product ID: 48951-1318_93f243c0-b964-9ea0-e053-2995a90aa852
• NDC: 48951-1318
• Product Type: Human Otc Drug
• Proprietary Name: Aurum 21X
• Generic Name: Aurum 21x
• 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: GOLD
• Active Ingredient Strength: 21 [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 48951-1318-1

10 AMPULE in 1 BOX (48951-1318-1) > 1 mL in 1 AMPULE

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

NDC SPL Data Element Entries

NDC 48951-1318-1 [48951131801]

Aurum 21X LIQUID

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

Drug Details

Active Ingredients

Ingredient	Strength
GOLD	21 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 93f243c0-b963-9ea0-e053-2995a90aa852
• Manufacturer:
  • Uriel Pharmacy Inc.
• UNII:
  • 79Y1949PYO