NDC 15631-0164

CUCURBITA CITRULLUS

Cucurbita Citrullus

CUCURBITA CITRULLUS 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 Watermelon Seed.

Product ID15631-0164_5c7fbef2-530b-4f90-8286-0d4ad7186d74
NDC15631-0164
Product TypeHuman Otc Drug
Proprietary NameCUCURBITA CITRULLUS
Generic NameCucurbita Citrullus
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-02
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameWATERMELON SEED
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0164-0

100 PELLET in 1 PACKAGE (15631-0164-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0164-2 [15631016402]

CUCURBITA CITRULLUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

NDC 15631-0164-3 [15631016403]

CUCURBITA CITRULLUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

NDC 15631-0164-1 [15631016401]

CUCURBITA CITRULLUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

NDC 15631-0164-0 [15631016400]

CUCURBITA CITRULLUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

NDC 15631-0164-5 [15631016405]

CUCURBITA CITRULLUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

NDC 15631-0164-4 [15631016404]

CUCURBITA CITRULLUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

Drug Details

Active Ingredients

IngredientStrength
WATERMELON SEED1 [hp_X]/1

OpenFDA Data

SPL SET ID:1f51c1a3-a0d8-4d8b-8a27-6c3dc794db0c
Manufacturer
UNII

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