NDC 15631-0302

MYRICA CERIFERA

Myrica Cerifera

MYRICA CERIFERA 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 Morella Cerifera Root Bark.

Product ID15631-0302_a1948856-8d3b-4ea2-e053-2995a90ade0f
NDC15631-0302
Product TypeHuman Otc Drug
Proprietary NameMYRICA CERIFERA
Generic NameMyrica Cerifera
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-10
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameMORELLA CERIFERA ROOT BARK
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0302-0

100 PELLET in 1 PACKAGE (15631-0302-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0302-1 [15631030201]

MYRICA CERIFERA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0302-2 [15631030202]

MYRICA CERIFERA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0302-4 [15631030204]

MYRICA CERIFERA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0302-0 [15631030200]

MYRICA CERIFERA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0302-3 [15631030203]

MYRICA CERIFERA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0302-5 [15631030205]

MYRICA CERIFERA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

Drug Details

Active Ingredients

IngredientStrength
MORELLA CERIFERA ROOT BARK1 [hp_X]/1

OpenFDA Data

SPL SET ID:a5141275-bb0c-4e10-a52e-2c3c70a51ed1
Manufacturer
UNII

NDC Crossover Matching brand name "MYRICA CERIFERA" or generic name "Myrica Cerifera"

NDCBrand NameGeneric Name
15631-0302MYRICA CERIFERAMYRICA CERIFERA
68428-518Myrica ceriferaMORELLA CERIFERA ROOT BARK
71919-473Myrica ceriferaMORELLA CERIFERA ROOT BARK

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