NDC 60512-6442

ACONITUM FEROX

Aconitum Ferox

ACONITUM FEROX is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Homeolab Usa Inc.. The primary component is Aconitum Ferox Root.

• Product ID: 60512-6442_4c5cf727-c17e-48bb-903f-cee51f84df0e
• NDC: 60512-6442
• Product Type: Human Otc Drug
• Proprietary Name: ACONITUM FEROX
• Generic Name: Aconitum Ferox
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 1995-10-11
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: HOMEOLAB USA INC.
• Substance Name: ACONITUM FEROX ROOT
• Active Ingredient Strength: 3 [hp_X]/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 60512-6442-1

80 PELLET in 1 TUBE (60512-6442-1)

• Marketing Start Date: 1995-10-11
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 60512-6442-1 [60512644201]

ACONITUM FEROX PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1995-10-11
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
ACONITUM FEROX ROOT	3 [hp_X]/1

OpenFDA Data

• SPL SET ID: b2df20c9-f3a5-4c60-990b-4bf4f506acbf
• Manufacturer:
  • HOMEOLAB USA INC.
• UNII:
  • I4G31A93ZR

NDC Crossover Matching brand name "ACONITUM FEROX" or generic name "Aconitum Ferox"

NDC	Brand Name	Generic Name
60512-6442	ACONITUM FEROX	ACONITUM FEROX
68428-176	Aconitum Ferox	ACONITUM FEROX ROOT
71919-007	Aconitum ferox	ACONITUM FEROX ROOT