NDC 48951-1129

Arnica e pl. tota 30

Arnica E Pl. Tota 30

Arnica e pl. tota 30 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: 48951-1129_6c7bf385-e03c-194f-e053-2991aa0a19bb
• NDC: 48951-1129
• Product Type: Human Otc Drug
• Proprietary Name: Arnica e pl. tota 30
• Generic Name: Arnica E Pl. Tota 30
• 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: 30 [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 48951-1129-1

10 AMPULE in 1 BOX (48951-1129-1) > 1 mL in 1 AMPULE

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

NDC SPL Data Element Entries

NDC 48951-1129-1 [48951112901]

Arnica e pl. tota 30 LIQUID

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

Drug Details

Active Ingredients

Ingredient	Strength
ARNICA MONTANA	30 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 540fcaa6-3baf-4b4a-8c0c-b213628d0256
• Manufacturer:
  • Uriel Pharmacy Inc.
• UNII:
  • O80TY208ZW

NDC Crossover Matching brand name "Arnica e pl. tota 30" or generic name "Arnica E Pl. Tota 30"

NDC	Brand Name	Generic Name
48951-1129	Arnica e pl. tota 30	Arnica e pl. tota 30
48951-1131	Arnica e pl. tota 30	Arnica e pl. tota 30