NDC 15631-0113

CASCARILLA

Cascarilla

CASCARILLA 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 Croton Eluteria Bark.

Product ID15631-0113_11c6bd68-40c2-41dd-bb63-8d79f4331897
NDC15631-0113
Product TypeHuman Otc Drug
Proprietary NameCASCARILLA
Generic NameCascarilla
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-02
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameCROTON ELUTERIA BARK
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0113-0

100 PELLET in 1 PACKAGE (15631-0113-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0113-4 [15631011304]

CASCARILLA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

NDC 15631-0113-1 [15631011301]

CASCARILLA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

NDC 15631-0113-2 [15631011302]

CASCARILLA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

NDC 15631-0113-0 [15631011300]

CASCARILLA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

NDC 15631-0113-3 [15631011303]

CASCARILLA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

NDC 15631-0113-5 [15631011305]

CASCARILLA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

Drug Details

Active Ingredients

IngredientStrength
CROTON ELUTERIA BARK1 [hp_X]/1

OpenFDA Data

SPL SET ID:11006a14-44be-40a5-b14a-f67cac2394df
Manufacturer
UNII

NDC Crossover Matching brand name "CASCARILLA" or generic name "Cascarilla"

NDCBrand NameGeneric Name
15631-0113CASCARILLACASCARILLA
68428-292CascarillaCROTON ELUTERIA BARK
71919-167CascarillaCROTON ELUTERIA BARK

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