NDC 63545-686

Plumeria Rubra

Plumeria Rubra

Plumeria Rubra is a Buccal; Oral; Sublingual Pellet in the Human Otc Drug category. It is labeled and distributed by Hahnemann Laboratories, Inc.. The primary component is Plumeria Rubra Whole.

• Product ID: 63545-686_4ebaa367-2c67-431b-e054-00144ff88e88
• NDC: 63545-686
• Product Type: Human Otc Drug
• Proprietary Name: Plumeria Rubra
• Generic Name: Plumeria Rubra
• Dosage Form: Pellet
• Route of Administration: BUCCAL; ORAL; SUBLINGUAL
• Marketing Start Date: 2017-05-04
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Hahnemann Laboratories, Inc.
• Substance Name: PLUMERIA RUBRA WHOLE
• Active Ingredient Strength: 30 [hp_C]/[hp_C]
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 63545-686-01

240 [hp_C] in 1 VIAL, GLASS (63545-686-01)

• Marketing Start Date: 2017-05-04
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 63545-686-01 [63545068601]

Plumeria Rubra PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2017-05-04
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
PLUMERIA RUBRA WHOLE	30 [hp_C]/[hp_C]

OpenFDA Data

• SPL SET ID: 4ebaa367-2c66-431b-e054-00144ff88e88
• Manufacturer:
  • Hahnemann Laboratories, Inc.
• UNII:
  • 31FL06Y50D