NDC 15631-0088

CACTUS GRANDIFLORUS

Cactus Grandiflorus

CACTUS GRANDIFLORUS 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 Selenicereus Grandiflorus Stem.

Product ID15631-0088_131844ca-7642-4c34-a8f6-d39f1f67c82d
NDC15631-0088
Product TypeHuman Otc Drug
Proprietary NameCACTUS GRANDIFLORUS
Generic NameCactus Grandiflorus
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-12
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameSELENICEREUS GRANDIFLORUS STEM
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0088-0

100 PELLET in 1 PACKAGE (15631-0088-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0088-1 [15631008801]

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

NDC 15631-0088-4 [15631008804]

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

NDC 15631-0088-3 [15631008803]

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

NDC 15631-0088-0 [15631008800]

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

NDC 15631-0088-5 [15631008805]

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

NDC 15631-0088-2 [15631008802]

CACTUS GRANDIFLORUS 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
SELENICEREUS GRANDIFLORUS STEM3 [hp_X]/1

OpenFDA Data

SPL SET ID:ed80f462-7a36-4c6d-a795-f67ff284355d
Manufacturer
UNII

NDC Crossover Matching brand name "CACTUS GRANDIFLORUS" or generic name "Cactus Grandiflorus"

NDCBrand NameGeneric Name
15631-0088CACTUS GRANDIFLORUSCACTUS GRANDIFLORUS
15631-0544CACTUS GRANDIFLORUSCACTUS GRANDIFLORUS
60512-6558CACTUS GRANDIFLORUSCACTUS GRANDIFLORUS
62106-7543CACTUS GRANDIFLORUSNight-blooming Cereus
63545-558Cactus GrandiflorusCactus Grandiflorus
63545-559Cactus GrandiflorusCactus Grandiflorus
63545-560Cactus GrandiflorusCactus Grandiflorus
63545-561Cactus GrandiflorusCactus Grandiflorus
63545-562Cactus GrandiflorusCactus Grandiflorus
63545-563Cactus GrandiflorusCactus Grandiflorus
63545-564Cactus GrandiflorusCactus Grandiflorus
63545-565Cactus GrandiflorusCactus Grandiflorus
63545-566Cactus GrandiflorusCactus Grandiflorus
68428-267Cactus grandiflorusSELENICEREUS GRANDIFLORUS STEM
71919-135Cactus grandiflorusSELENICEREUS GRANDIFLORUS STEM
79718-1137Cactus GrandiflorusCactus Grandiflorus
69152-1022Cactus grandiflorus 200CCactus grandiflorus
69152-1099Cactus grandiflorus 30CCactus grandiflorus

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