NDC 0220-3339

Melissa officinalis

Melissa Officinalis

Melissa officinalis is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Boiron. The primary component is Melissa Officinalis.

• Product ID: 0220-3339_7d79baea-28c4-4d41-e053-2991aa0a5269
• NDC: 0220-3339
• Product Type: Human Otc Drug
• Proprietary Name: Melissa officinalis
• Generic Name: Melissa Officinalis
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 1983-03-03
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Boiron
• Substance Name: MELISSA OFFICINALIS
• Active Ingredient Strength: 30 [hp_C]/30[hp_C]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 0220-3339-41

30 [hp_C] in 1 TUBE (0220-3339-41)

• Marketing Start Date: 1983-03-03
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0220-3339-41 [00220333941]

Melissa officinalis PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1983-03-03

Drug Details

Active Ingredients

Ingredient	Strength
MELISSA OFFICINALIS	30 [hp_C]/30[hp_C]

OpenFDA Data

• SPL SET ID: 7d79baea-28c3-4d41-e053-2991aa0a5269
• Manufacturer:
  • Boiron
• UNII:
  • YF70189L0N

NDC Crossover Matching brand name "Melissa officinalis" or generic name "Melissa Officinalis"

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