NDC 60512-6055

CORALLIUM RUBRUM

Corallium Rubrum

CORALLIUM RUBRUM is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Homeolab Usa Inc.. The primary component is Corallium Rubrum Exoskeleton.

• Product ID: 60512-6055_1057b468-8692-456d-a852-e84c23859fd0
• NDC: 60512-6055
• Product Type: Human Otc Drug
• Proprietary Name: CORALLIUM RUBRUM
• Generic Name: Corallium Rubrum
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 1995-10-11
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: HOMEOLAB USA INC.
• Substance Name: CORALLIUM RUBRUM EXOSKELETON
• Active Ingredient Strength: 8 [hp_X]/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 60512-6055-1

80 PELLET in 1 TUBE (60512-6055-1)

• Marketing Start Date: 1995-10-11
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 60512-6055-1 [60512605501]

CORALLIUM RUBRUM PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1995-10-11
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
CORALLIUM RUBRUM EXOSKELETON	8 [hp_X]/1

OpenFDA Data

• SPL SET ID: 42f17563-9d38-4f78-803d-40e05a177e7c
• Manufacturer:
  • HOMEOLAB USA INC.
• UNII:
  • 2CA71K0DLE

NDC Crossover Matching brand name "CORALLIUM RUBRUM" or generic name "Corallium Rubrum"

NDC	Brand Name	Generic Name
0220-1541	Corallium rubrum	CORALLIUM RUBRUM EXOSKELETON
15631-0157	CORALLIUM RUBRUM	CORALLIUM RUBRUM
60512-6055	CORALLIUM RUBRUM	CORALLIUM RUBRUM
68428-341	Corallium rubrum	CORALLIUM RUBRUM EXOSKELETON
71919-229	Corallium rubrum	CORALLIUM RUBRUM EXOSKELETON