NDC 63545-657

Cinnamomum

Cinnamomum

Cinnamomum 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 Cinnamon.

• Product ID: 63545-657_44bb1b0d-6f06-32f5-e054-00144ff8d46c
• NDC: 63545-657
• Product Type: Human Otc Drug
• Proprietary Name: Cinnamomum
• Generic Name: Cinnamomum
• Dosage Form: Pellet
• Route of Administration: BUCCAL; ORAL; SUBLINGUAL
• Marketing Start Date: 2016-12-01
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Hahnemann Laboratories, Inc.
• Substance Name: CINNAMON
• Active Ingredient Strength: 30 [hp_C]/[hp_C]
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 63545-657-01

240 [hp_C] in 1 VIAL, GLASS (63545-657-01)

• Marketing Start Date: 2016-12-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 63545-657-01 [63545065701]

Cinnamomum PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-12-01
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
CINNAMON	30 [hp_C]/[hp_C]

OpenFDA Data

• SPL SET ID: 44bb1b0d-6f05-32f5-e054-00144ff8d46c
• Manufacturer:
  • Hahnemann Laboratories, Inc.
• UNII:
  • 5S29HWU6QB

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

NDC	Brand Name	Generic Name
0220-1406	Cinnamomum	CINNAMON
15631-0140	CINNAMOMUM	CINNAMOMUM
37662-0329	Cinnamomum	Cinnamomum
37662-0330	Cinnamomum	Cinnamomum
37662-0331	Cinnamomum	Cinnamomum
37662-0332	Cinnamomum	Cinnamomum
37662-0333	Cinnamomum	Cinnamomum
37662-0334	Cinnamomum	Cinnamomum
37662-0335	Cinnamomum	Cinnamomum
63545-657	Cinnamomum	Cinnamomum
68428-322	Cinnamomum	CINNAMON
71919-204	Cinnamomum	CINNAMON