NDC 48951-1132

Arnica e pl. tota 6

Arnica E Pl. Tota 6

Arnica e pl. tota 6 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: 48951-1132_54997f39-b3e2-60a0-e054-00144ff8d46c
• NDC: 48951-1132
• Product Type: Human Otc Drug
• Proprietary Name: Arnica e pl. tota 6
• Generic Name: Arnica E Pl. Tota 6
• 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: 6 [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 48951-1132-1

10 AMPULE in 1 BOX (48951-1132-1) > 1 mL in 1 AMPULE

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

NDC SPL Data Element Entries

NDC 48951-1132-1 [48951113201]

Arnica e pl. tota 6 LIQUID

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

Drug Details

Active Ingredients

Ingredient	Strength
ARNICA MONTANA	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: d84176b5-8e86-4055-abf5-f4a80ad4334f
• Manufacturer:
  • Uriel Pharmacy Inc.
• UNII:
  • O80TY208ZW

NDC Crossover Matching brand name "Arnica e pl. tota 6" or generic name "Arnica E Pl. Tota 6"

NDC	Brand Name	Generic Name
48951-1132	Arnica e pl. tota 6	Arnica e pl. tota 6
48951-1134	Arnica e pl. tota 6	Arnica e pl. tota 6
48951-8308	Arnica e pl. tota 6	Arnica e pl. tota 6