NDC 15631-0568

COLLINSONIA CANADENSIS

Collinsonia Canadensis

COLLINSONIA CANADENSIS 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 Collinsonia Canadensis Root.

Product ID15631-0568_d525bd64-41c6-4751-979d-586f69efe1f0
NDC15631-0568
Product TypeHuman Otc Drug
Proprietary NameCOLLINSONIA CANADENSIS
Generic NameCollinsonia Canadensis
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-12-27
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameCOLLINSONIA CANADENSIS ROOT
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0568-4

250 TABLET in 1 CONTAINER (15631-0568-4)
Marketing Start Date2015-12-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0568-4 [15631056804]

COLLINSONIA CANADENSIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0568-2 [15631056802]

COLLINSONIA CANADENSIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0568-0 [15631056800]

COLLINSONIA CANADENSIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0568-1 [15631056801]

COLLINSONIA CANADENSIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0568-3 [15631056803]

COLLINSONIA CANADENSIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0568-5 [15631056805]

COLLINSONIA CANADENSIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0568-7 [15631056807]

COLLINSONIA CANADENSIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0568-6 [15631056806]

COLLINSONIA CANADENSIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
COLLINSONIA CANADENSIS ROOT1 [hp_X]/1

OpenFDA Data

SPL SET ID:7812c9c1-ccbf-49a7-8e23-d88629b29baf
Manufacturer
UNII
UPC Code
  • 8907460005526

    • NDC Crossover Matching brand name "COLLINSONIA CANADENSIS" or generic name "Collinsonia Canadensis"

    NDCBrand NameGeneric Name
    0220-1485Collinsonia canadensisCOLLINSONIA CANADENSIS ROOT
    0220-1489Collinsonia canadensisCOLLINSONIA CANADENSIS ROOT
    0220-1492Collinsonia canadensisCOLLINSONIA CANADENSIS ROOT
    15631-0151COLLINSONIA CANADENSISCOLLINSONIA CANADENSIS
    15631-0568COLLINSONIA CANADENSISCOLLINSONIA CANADENSIS
    37662-0481Collinsonia CanadensisCollinsonia Canadensis
    37662-0482Collinsonia CanadensisCollinsonia Canadensis
    37662-0483Collinsonia CanadensisCollinsonia Canadensis
    37662-0484Collinsonia CanadensisCollinsonia Canadensis
    37662-0485Collinsonia CanadensisCollinsonia Canadensis
    37662-0486Collinsonia CanadensisCollinsonia Canadensis
    37662-0487Collinsonia CanadensisCollinsonia Canadensis
    37662-0488Collinsonia CanadensisCollinsonia Canadensis
    60512-6614COLLINSONIA CANADENSISCOLLINSONIA CANADENSIS
    68428-334Collinsonia canadensisCOLLINSONIA CANADENSIS ROOT
    71919-220Collinsonia canadensisCOLLINSONIA CANADENSIS ROOT
    69152-1115Collinsonia canadensis 200CCollinsonia canadensis
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