NDC 0220-1541

Corallium rubrum

Corallium Rubrum Exoskeleton

Corallium rubrum is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Boiron. The primary component is Corallium Rubrum Exoskeleton.

• Product ID: 0220-1541_7a2d4904-d2b2-ef74-e053-2a91aa0a284a
• NDC: 0220-1541
• Product Type: Human Otc Drug
• Proprietary Name: Corallium rubrum
• Generic Name: Corallium Rubrum Exoskeleton
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 1983-03-03
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Boiron
• Substance Name: CORALLIUM RUBRUM EXOSKELETON
• Active Ingredient Strength: 5 [hp_C]/5[hp_C]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 0220-1541-41

5 [hp_C] in 1 TUBE (0220-1541-41)

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

NDC SPL Data Element Entries

NDC 0220-1541-41 [00220154141]

Corallium rubrum PELLET

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

Drug Details

Active Ingredients

Ingredient	Strength
CORALLIUM RUBRUM EXOSKELETON	5 [hp_C]/5[hp_C]

OpenFDA Data

• SPL SET ID: 7a2d4904-d2b1-ef74-e053-2a91aa0a284a
• Manufacturer:
  • Boiron
• UNII:
  • 2CA71K0DLE

NDC Crossover Matching brand name "Corallium rubrum" or generic name "Corallium Rubrum Exoskeleton"

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