NDC 53645-1610

Aconitum

Aconitum

Aconitum is a Oral Globule in the Human Otc Drug category. It is labeled and distributed by True Botanica, Llc. The primary component is Aconitum Napellus Root.

• Product ID: 53645-1610_61870547-8bb4-35ff-e053-2a91aa0a2a50
• NDC: 53645-1610
• Product Type: Human Otc Drug
• Proprietary Name: Aconitum
• Generic Name: Aconitum
• Dosage Form: Globule
• Route of Administration: ORAL
• Marketing Start Date: 2017-11-24
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: True Botanica, LLC
• Substance Name: ACONITUM NAPELLUS ROOT
• Active Ingredient Strength: 30 [hp_X]/23g
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 53645-1610-2

23 g in 1 BOTTLE (53645-1610-2)

• Marketing Start Date: 2017-11-24
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 53645-1610-2 [53645161002]

Aconitum GLOBULE

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2017-11-24

Drug Details

Active Ingredients

Ingredient	Strength
ACONITUM NAPELLUS ROOT	30 [hp_X]/23g

OpenFDA Data

• SPL SET ID: 61870547-8bb3-35ff-e053-2a91aa0a2a50
• Manufacturer:
  • True Botanica, LLC
• UNII:
  • KPD2N7348X

NDC Crossover Matching brand name "Aconitum" or generic name "Aconitum"

NDC	Brand Name	Generic Name
0360-0005	ACONITUM	ACONITUM NAPELLUS
53645-1610	Aconitum	Aconitum