NDC 15631-0205

GENTIANA QUINQUEFLORA

Gentiana Quinqueflora

GENTIANA QUINQUEFLORA 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 Gentianella Quinquefolia.

Product ID15631-0205_a144c9b3-7f2c-8965-e053-2995a90a5cb0
NDC15631-0205
Product TypeHuman Otc Drug
Proprietary NameGENTIANA QUINQUEFLORA
Generic NameGentiana Quinqueflora
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-27
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameGENTIANELLA QUINQUEFOLIA
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0205-0

100 PELLET in 1 PACKAGE (15631-0205-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0205-2 [15631020502]

GENTIANA QUINQUEFLORA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0205-4 [15631020504]

GENTIANA QUINQUEFLORA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0205-1 [15631020501]

GENTIANA QUINQUEFLORA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0205-3 [15631020503]

GENTIANA QUINQUEFLORA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0205-5 [15631020505]

GENTIANA QUINQUEFLORA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0205-0 [15631020500]

GENTIANA QUINQUEFLORA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

Drug Details

Active Ingredients

IngredientStrength
GENTIANELLA QUINQUEFOLIA1 [hp_X]/1

OpenFDA Data

SPL SET ID:22e7d392-fe72-4f4f-876b-318ec90bdcda
Manufacturer
UNII

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