NDC 15631-0429

TARENTULA CUBENSIS

Tarentula Cubensis

TARENTULA CUBENSIS 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 Citharacanthus Spinicrus.

Product ID15631-0429_8351becd-4461-4e5e-800e-dd8c5afbc26b
NDC15631-0429
Product TypeHuman Otc Drug
Proprietary NameTARENTULA CUBENSIS
Generic NameTarentula Cubensis
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-11-06
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameCITHARACANTHUS SPINICRUS
Active Ingredient Strength8 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0429-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0429-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0429-4 [15631042904]

TARENTULA CUBENSIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0429-3 [15631042903]

TARENTULA CUBENSIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0429-0 [15631042900]

TARENTULA CUBENSIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0429-5 [15631042905]

TARENTULA CUBENSIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0429-1 [15631042901]

TARENTULA CUBENSIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0429-2 [15631042902]

TARENTULA CUBENSIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

Drug Details

Active Ingredients

IngredientStrength
CITHARACANTHUS SPINICRUS8 [hp_X]/1

OpenFDA Data

SPL SET ID:e7e2cda3-7b3b-4531-ab46-69a72b3b6b26
Manufacturer
UNII

NDC Crossover Matching brand name "TARENTULA CUBENSIS" or generic name "Tarentula Cubensis"

NDCBrand NameGeneric Name
0220-4937Tarentula cubensisCITHARACANTHUS SPINICRUS
0220-4938Tarentula cubensisCITHARACANTHUS SPINICRUS
15631-0429TARENTULA CUBENSISTARENTULA CUBENSIS
15631-0430TARENTULA CUBENSISTARENTULA CUBENSIS
68428-664Tarentula cubensisCITHARACANTHUS SPINICRUS
71919-666TARENTULA CUBENSISCitharacanthus spinicrus

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