NDC 15631-0157

CORALLIUM RUBRUM

Corallium Rubrum

CORALLIUM RUBRUM is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc. The primary component is Corallium Rubrum Exoskeleton.

Product ID15631-0157_5cea9493-f4d7-471d-b6a4-63030956f298
NDC15631-0157
Product TypeHuman Otc Drug
Proprietary NameCORALLIUM RUBRUM
Generic NameCorallium Rubrum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-06
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameCORALLIUM RUBRUM EXOSKELETON
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0157-0

100 PELLET in 1 PACKAGE (15631-0157-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0157-3 [15631015703]

CORALLIUM RUBRUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

NDC 15631-0157-2 [15631015702]

CORALLIUM RUBRUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

NDC 15631-0157-4 [15631015704]

CORALLIUM RUBRUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

NDC 15631-0157-0 [15631015700]

CORALLIUM RUBRUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

NDC 15631-0157-1 [15631015701]

CORALLIUM RUBRUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

NDC 15631-0157-5 [15631015705]

CORALLIUM RUBRUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

Drug Details

Active Ingredients

IngredientStrength
CORALLIUM RUBRUM EXOSKELETON1 [hp_X]/1

OpenFDA Data

SPL SET ID:1abdf36c-dd25-4117-88fa-7a4f746ea427
Manufacturer
UNII

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

NDCBrand NameGeneric Name
0220-1541Corallium rubrumCORALLIUM RUBRUM EXOSKELETON
15631-0157CORALLIUM RUBRUMCORALLIUM RUBRUM
60512-6055CORALLIUM RUBRUMCORALLIUM RUBRUM
68428-341Corallium rubrumCORALLIUM RUBRUM EXOSKELETON
71919-229Corallium rubrumCORALLIUM RUBRUM EXOSKELETON

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