NDC 48951-1267

Arnica e pl. tota 10

Arnica E Pl. Tota 10

Arnica e pl. tota 10 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.

• Product ID: 48951-1267_4c1fdc15-a4c8-4036-8fe5-d3115eebcfc7
• NDC: 48951-1267
• Product Type: Human Otc Drug
• Proprietary Name: Arnica e pl. tota 10
• Generic Name: Arnica E Pl. Tota 10
• 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
• Active Ingredient Strength: 10 [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 48951-1267-1

10 AMPULE in 1 BOX (48951-1267-1) > 1 mL in 1 AMPULE

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

NDC SPL Data Element Entries

NDC 48951-1267-1 [48951126701]

Arnica e pl. tota 10 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	10 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 77780be3-2456-46cc-91c0-77b50e8743ca
• Manufacturer:
  • Uriel Pharmacy Inc.
• UNII:
  • O80TY208ZW