NDC 10191-1249

ARNICA MONTANA WHOLE PLANT

(whole Plant)

ARNICA MONTANA WHOLE PLANT is a Sublingual Pellet in the Human Otc Drug category. It is labeled and distributed by Remedy Makers. The primary component is Arnica Montana.

• Product ID: 10191-1249_78abcbc1-e124-46c1-9402-4c16650a05ef
• NDC: 10191-1249
• Product Type: Human Otc Drug
• Proprietary Name: ARNICA MONTANA WHOLE PLANT
• Generic Name: (whole Plant)
• Dosage Form: Pellet
• Route of Administration: SUBLINGUAL
• Marketing Start Date: 2005-08-24
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Remedy Makers
• Substance Name: ARNICA MONTANA
• Active Ingredient Strength: 6 [hp_C]/1
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 10191-1249-2

155 PELLET in 1 VIAL, GLASS (10191-1249-2)

• Marketing Start Date: 2005-08-24
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 10191-1249-2 [10191124902]

ARNICA MONTANA WHOLE PLANT PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2005-08-24
• Inactivation Date: 2019-10-21

Drug Details

Active Ingredients

Ingredient	Strength
ARNICA MONTANA	6 [hp_C]/1

OpenFDA Data

• SPL SET ID: cdba7652-e3af-40fa-b777-89c88e2a6a5e
• Manufacturer:
  • Remedy Makers
• UNII:
  • O80TY208ZW
• UPC Code:
  • 0310191124929

NDC Crossover Matching brand name "ARNICA MONTANA WHOLE PLANT" or generic name "(whole Plant)"

NDC	Brand Name	Generic Name
10191-1249	ARNICA MONTANA WHOLE PLANT	(WHOLE PLANT)
10191-1253	ARNICA MONTANA WHOLE PLANT	WHOLE ARNICA PLANT