NDC 15631-0569

COLOCYNTHIS

Colocynthis

COLOCYNTHIS is a Oral Tablet 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 ID15631-0569_156ae625-259f-44cd-85fa-c131f5e5b182
NDC15631-0569
Product TypeHuman Otc Drug
Proprietary NameCOLOCYNTHIS
Generic NameColocynthis
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-12-27
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 FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0569-5

500 TABLET in 1 CONTAINER (15631-0569-5)
Marketing Start Date2015-12-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0569-3 [15631056903]

COLOCYNTHIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0569-1 [15631056901]

COLOCYNTHIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0569-6 [15631056906]

COLOCYNTHIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0569-0 [15631056900]

COLOCYNTHIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0569-7 [15631056907]

COLOCYNTHIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0569-5 [15631056905]

COLOCYNTHIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0569-4 [15631056904]

COLOCYNTHIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0569-2 [15631056902]

COLOCYNTHIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
CITRULLUS COLOCYNTHIS FRUIT PULP3 [hp_X]/1

OpenFDA Data

SPL SET ID:31bd87a8-e243-4e50-be2f-77e704ef9581
Manufacturer
UNII
UPC Code
  • 8907460005526
  • 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

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.