NDC 13838-1444

Melilotus officinalis (N)

Melilotus Officinalis Top

Melilotus officinalis (N) is a Oral Tincture in the Human Otc Drug category. It is labeled and distributed by Phytodyne Inc.. The primary component is Melilotus Officinalis Top.

• Product ID: 13838-1444_0b5017bd-f1ce-49b6-bfa2-4801e5f7384e
• NDC: 13838-1444
• Product Type: Human Otc Drug
• Proprietary Name: Melilotus officinalis (N)
• Generic Name: Melilotus Officinalis Top
• Dosage Form: Tincture
• Route of Administration: ORAL
• Marketing Start Date: 2005-10-01
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Phytodyne Inc.
• Substance Name: MELILOTUS OFFICINALIS TOP
• Active Ingredient Strength: 1 [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2022-12-31

Packaging

NDC 13838-1444-1

20 mL in 1 BOTTLE, GLASS (13838-1444-1)

• Marketing Start Date: 2005-10-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 13838-1444-1 [13838144401]

Melilotus officinalis (N) TINCTURE

• Marketing Category: Unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2005-10-01

Drug Details

Active Ingredients

Ingredient	Strength
MELILOTUS OFFICINALIS TOP	1 [hp_X]/mL

OpenFDA Data

• SPL SET ID: e567b869-0c19-41e2-b81b-fde4a765ba5d
• Manufacturer:
  • Phytodyne Inc.
• UNII:
  • GM6P02J2DX

NDC Crossover Matching brand name "Melilotus officinalis (N)" or generic name "Melilotus Officinalis Top"

NDC	Brand Name	Generic Name
13838-1444	Melilotus officinalis (N)	melilotus officinalis top
64117-162	Headache Spasms	MELILOTUS OFFICINALIS TOP
68428-496	Melilotus alba	MELILOTUS OFFICINALIS TOP
0220-3335	Melilotus officinalis	MELILOTUS OFFICINALIS TOP
68428-497	Melilotus officinalis	MELILOTUS OFFICINALIS TOP
71919-447	Melilotus officinalis	MELILOTUS OFFICINALIS TOP