NDC 15631-0151

COLLINSONIA CANADENSIS

Collinsonia Canadensis

COLLINSONIA CANADENSIS 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 Collinsonia Canadensis Root.

Product ID15631-0151_a108492b-d278-3d4b-e053-2995a90a856b
NDC15631-0151
Product TypeHuman Otc Drug
Proprietary NameCOLLINSONIA CANADENSIS
Generic NameCollinsonia Canadensis
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 NameCOLLINSONIA CANADENSIS ROOT
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0151-0

100 PELLET in 1 PACKAGE (15631-0151-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0151-3 [15631015103]

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

NDC 15631-0151-0 [15631015100]

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

NDC 15631-0151-1 [15631015101]

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

NDC 15631-0151-4 [15631015104]

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

NDC 15631-0151-5 [15631015105]

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

NDC 15631-0151-2 [15631015102]

COLLINSONIA CANADENSIS 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
COLLINSONIA CANADENSIS ROOT1 [hp_X]/1

OpenFDA Data

SPL SET ID:8728f137-cd88-4e75-ac69-8cf87fa7f257
Manufacturer
UNII

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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