NDC 60512-6445

ACONITUM, RADIX

Aconitum, Radix

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

• Product ID: 60512-6445_8202e548-8750-4c6b-8ec6-d2183f613565
• NDC: 60512-6445
• Product Type: Human Otc Drug
• Proprietary Name: ACONITUM, RADIX
• Generic Name: Aconitum, Radix
• 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 NAPELLUS ROOT
• Active Ingredient Strength: 6 [hp_X]/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 60512-6445-1

80 PELLET in 1 TUBE (60512-6445-1)

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

NDC SPL Data Element Entries

NDC 60512-6445-1 [60512644501]

ACONITUM, RADIX 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 NAPELLUS ROOT	6 [hp_X]/1

OpenFDA Data

• SPL SET ID: a06eebe7-2fa3-4fc2-bc7b-ebbb6945645c
• Manufacturer:
  • HOMEOLAB USA INC.
• UNII:
  • KPD2N7348X

NDC Crossover Matching brand name "ACONITUM, RADIX" or generic name "Aconitum, Radix"

NDC	Brand Name	Generic Name
60512-6445	ACONITUM, RADIX	ACONITUM, RADIX
68428-865	Aconitum, radix	ACONITUM NAPELLUS ROOT