NDC 15631-0152

COLOCYNTHIS

Colocynthis

COLOCYNTHIS 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 Citrullus Colocynthis Fruit Pulp.

Product ID15631-0152_a1085fec-115d-abfb-e053-2a95a90abfeb
NDC15631-0152
Product TypeHuman Otc Drug
Proprietary NameCOLOCYNTHIS
Generic NameColocynthis
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 NameCITRULLUS COLOCYNTHIS FRUIT PULP
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0152-0

100 PELLET in 1 PACKAGE (15631-0152-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0152-3 [15631015203]

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

NDC 15631-0152-2 [15631015202]

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

NDC 15631-0152-4 [15631015204]

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

NDC 15631-0152-5 [15631015205]

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

NDC 15631-0152-1 [15631015201]

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

NDC 15631-0152-0 [15631015200]

COLOCYNTHIS 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
CITRULLUS COLOCYNTHIS FRUIT PULP3 [hp_X]/1

OpenFDA Data

SPL SET ID:5ec7c1d2-7d5f-4cbe-ac5a-c4d8242a7a5b
Manufacturer
UNII

NDC Crossover Matching brand name "COLOCYNTHIS" or generic name "Colocynthis"

NDCBrand NameGeneric Name
0220-1496ColocynthisCITRULLUS COLOCYNTHIS FRUIT PULP
0220-1499ColocynthisCITRULLUS COLOCYNTHIS FRUIT PULP
0220-1502ColocynthisCITRULLUS COLOCYNTHIS FRUIT PULP
0220-1503ColocynthisCITRULLUS COLOCYNTHIS FRUIT PULP
0220-1506ColocynthisCITRULLUS COLOCYNTHIS FRUIT PULP
0220-1507ColocynthisCITRULLUS COLOCYNTHIS FRUIT PULP
0220-1510ColocynthisCITRULLUS COLOCYNTHIS FRUIT PULP
0220-1514ColocynthisCITRULLUS COLOCYNTHIS FRUIT PULP
0220-1515ColocynthisCITRULLUS COLOCYNTHIS FRUIT PULP
0360-0145COLOCYNTHISCOLOCYNTHIS
0360-0146COLOCYNTHISCOLOCYNTHIS
15631-0152COLOCYNTHISCOLOCYNTHIS
15631-0569COLOCYNTHISCOLOCYNTHIS
37662-0520ColocynthisColocynthis
37662-0521ColocynthisColocynthis
37662-0522ColocynthisColocynthis
37662-0523ColocynthisColocynthis
37662-0524ColocynthisColocynthis
37662-0525ColocynthisColocynthis
37662-0526ColocynthisColocynthis
37662-0527ColocynthisColocynthis
37662-0528ColocynthisColocynthis
60512-1014COLOCYNTHISCOLOCYNTHIS
60512-6615COLOCYNTHISCOLOCYNTHIS
62106-7747COLOCYNTHISColocynth
66096-823ColocynthisCOLOCYNTHIS
68428-335ColocynthisCITRULLUS COLOCYNTHIS FRUIT PULP
71919-221ColocynthisCITRULLUS COLOCYNTHIS FRUIT PULP
76472-4045COLOCYNTHISCOLOCYNTHIS
76472-4077COLOCYNTHISCOLOCYNTHIS
69152-1016Colocynthis 200CColocynthis

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