NDC 60512-7120

COCCUS CACTI

Coccus Cacti

COCCUS CACTI is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Homeolab Usa Inc.. The primary component is Dactylopius Coccus Whole.

Product ID60512-7120_f72d8665-37bd-4543-a919-23b6556c5057
NDC60512-7120
Product TypeHuman Otc Drug
Proprietary NameCOCCUS CACTI
Generic NameCoccus Cacti
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date1995-10-11
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameHOMEOLAB USA INC.
Substance NameDACTYLOPIUS COCCUS WHOLE
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 60512-7120-1

80 PELLET in 1 TUBE (60512-7120-1)
Marketing Start Date1995-10-11
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 60512-7120-1 [60512712001]

COCCUS CACTI PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date1995-10-11
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
DACTYLOPIUS COCCUS WHOLE1 [hp_X]/1

OpenFDA Data

SPL SET ID:684e8aa4-96eb-4a6e-9f64-405312a2b29b
Manufacturer
UNII

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

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