NDC 15631-0566

COCCUS CACTI

Coccus Cacti

COCCUS CACTI 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 Protortonia Cacti.

Product ID15631-0566_1d1147de-d732-4bb0-b5c7-64f0082513d5
NDC15631-0566
Product TypeHuman Otc Drug
Proprietary NameCOCCUS CACTI
Generic NameCoccus Cacti
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 NamePROTORTONIA CACTI
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0566-5

500 TABLET in 1 CONTAINER (15631-0566-5)
Marketing Start Date2015-12-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0566-4 [15631056604]

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

NDC 15631-0566-2 [15631056602]

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

NDC 15631-0566-0 [15631056600]

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

NDC 15631-0566-5 [15631056605]

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

NDC 15631-0566-6 [15631056606]

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

NDC 15631-0566-3 [15631056603]

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

NDC 15631-0566-1 [15631056601]

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

NDC 15631-0566-7 [15631056607]

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

Drug Details

Active Ingredients

IngredientStrength
PROTORTONIA CACTI1 [hp_X]/1

OpenFDA Data

SPL SET ID:b6a1f5e5-27dc-4acf-a467-da668244e82e
Manufacturer
UNII
UPC Code
  • 8907460005526
  • NDC Crossover Matching brand name "COCCUS CACTI" or generic name "Coccus Cacti"

    NDCBrand NameGeneric Name
    0220-1463Coccus cactiPROTORTONIA CACTI
    0220-1464Coccus cactiPROTORTONIA CACTI
    0220-1465Coccus cactiPROTORTONIA CACTI
    15631-0146COCCUS CACTICOCCUS CACTI
    15631-0566COCCUS CACTICOCCUS CACTI
    37662-0489Coccus CactiCoccus Cacti
    37662-0490Coccus CactiCoccus Cacti
    37662-0491Coccus CactiCoccus Cacti
    37662-0492Coccus CactiCoccus Cacti
    37662-0493Coccus CactiCoccus Cacti
    37662-0494Coccus CactiCoccus Cacti
    37662-0495Coccus CactiCoccus Cacti
    37662-0496Coccus CactiCoccus Cacti
    37662-0497Coccus CactiCoccus Cacti
    60512-7120COCCUS CACTICOCCUS CACTI
    62106-6615COCCUS CACTICochineal
    66096-821Coccus CactiCOCCUS CACTI
    68428-330Coccus cactiPROTORTONIA CACTI
    71919-213Coccus cactiPROTORTONIA CACTI

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