NDC 15631-0595

GUAIACUM

Guaiacum

GUAIACUM is a Oral Tablet 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 ID15631-0595_cf3312d5-aeda-465b-b507-2a37ca981b59
NDC15631-0595
Product TypeHuman Otc Drug
Proprietary NameGUAIACUM
Generic NameGuaiacum
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2016-01-07
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 15631-0595-5

500 TABLET in 1 CONTAINER (15631-0595-5)
Marketing Start Date2016-01-07
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0595-1 [15631059501]

GUAIACUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-07
Inactivation Date2020-01-31

NDC 15631-0595-3 [15631059503]

GUAIACUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-07
Inactivation Date2020-01-31

NDC 15631-0595-5 [15631059505]

GUAIACUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-07
Inactivation Date2020-01-31

NDC 15631-0595-2 [15631059502]

GUAIACUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-07
Inactivation Date2020-01-31

NDC 15631-0595-6 [15631059506]

GUAIACUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-07
Inactivation Date2020-01-31

NDC 15631-0595-4 [15631059504]

GUAIACUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-07
Inactivation Date2020-01-31

NDC 15631-0595-0 [15631059500]

GUAIACUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-07
Inactivation Date2020-01-31

NDC 15631-0595-7 [15631059507]

GUAIACUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-07
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
GUAIACUM OFFICINALE RESIN1 [hp_X]/1

OpenFDA Data

SPL SET ID:00e707fd-4aa9-44cf-bdb6-1216aa517cca
Manufacturer
UNII
UPC Code
  • 8907460005526
  • 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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