NDC 48951-1136

Arnica e rad. 20

Arnica E Rad. 20

Arnica e rad. 20 is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc.. The primary component is Arnica Montana Root.

• Product ID: 48951-1136_3b5c07cd-3c77-402e-aac1-a33c5214a055
• NDC: 48951-1136
• Product Type: Human Otc Drug
• Proprietary Name: Arnica e rad. 20
• Generic Name: Arnica E Rad. 20
• 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: ARNICA MONTANA ROOT
• Active Ingredient Strength: 20 [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 48951-1136-1

10 AMPULE in 1 BOX (48951-1136-1) > 1 mL in 1 AMPULE

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

NDC SPL Data Element Entries

NDC 48951-1136-1 [48951113601]

Arnica e rad. 20 LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2009-09-01
• Marketing End Date: 2019-11-25

Drug Details

Active Ingredients

Ingredient	Strength
ARNICA MONTANA ROOT	20 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 8b06f2e3-595d-4d22-9323-900ab6dabf6b
• Manufacturer:
  • Uriel Pharmacy Inc.
• UNII:
  • MUE8Y11327