NDC 13838-1451

Melissa officinalis (N)

Melissa Officinalis

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

• Product ID: 13838-1451_56eae30a-5293-4a61-9850-c53363d3af82
• NDC: 13838-1451
• Product Type: Human Otc Drug
• Proprietary Name: Melissa officinalis (N)
• Generic Name: Melissa Officinalis
• 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: MELISSA OFFICINALIS LEAF
• Active Ingredient Strength: 1 [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 13838-1451-1

20 mL in 1 BOTTLE, GLASS (13838-1451-1)

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

NDC SPL Data Element Entries

NDC 13838-1451-1 [13838145101]

Melissa officinalis (N) TINCTURE

• Marketing Category: UNAPPROVED HOMEOPATHIC
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2005-10-01

Drug Details

Active Ingredients

Ingredient	Strength
MELISSA OFFICINALIS LEAF	1 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 5ee85b4e-053b-4b56-b971-bbf619e8ecd7
• Manufacturer:
  • Phytodyne Inc.
• UNII:
  • 50D2ZE9219

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

NDC	Brand Name	Generic Name
13838-1451	Melissa officinalis (N)	Melissa officinalis
0220-3339	Melissa officinalis	MELISSA OFFICINALIS
68428-498	Melissa officinalis	MELISSA OFFICINALIS
71919-448	Melissa officinalis	MELISSA OFFICINALIS