NDC 15631-0214

GUAIACUM

Guaiacum

GUAIACUM 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 Guaiacum Officinale Resin.

Product ID15631-0214_3cdcd82f-c079-4b71-83bb-4b13439fab43
NDC15631-0214
Product TypeHuman Otc Drug
Proprietary NameGUAIACUM
Generic NameGuaiacum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-31
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameGUAIACUM OFFICINALE RESIN
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0214-0

100 PELLET in 1 PACKAGE (15631-0214-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0214-2 [15631021402]

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

NDC 15631-0214-3 [15631021403]

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

NDC 15631-0214-1 [15631021401]

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

NDC 15631-0214-4 [15631021404]

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

NDC 15631-0214-5 [15631021405]

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

NDC 15631-0214-0 [15631021400]

GUAIACUM 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
GUAIACUM OFFICINALE RESIN1 [hp_X]/1

OpenFDA Data

SPL SET ID:4e4d14c5-e736-4989-8a2f-0574781c5cac
Manufacturer
UNII

NDC Crossover Matching brand name "GUAIACUM" or generic name "Guaiacum"

NDCBrand NameGeneric Name
15631-0214GUAIACUMGUAIACUM
15631-0595GUAIACUMGUAIACUM
37662-1482GuaiacumGuaiacum
37662-1483GuaiacumGuaiacum
37662-1484GuaiacumGuaiacum
37662-1485GuaiacumGuaiacum
37662-1486GuaiacumGuaiacum
37662-1487GuaiacumGuaiacum
37662-1488GuaiacumGuaiacum
68428-415GuaiacumGUAIACUM OFFICINALE RESIN
71919-328GuaiacumGUAIACUM OFFICINALE RESIN

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