NDC 15631-0389

SANGUINARIA CANADENSIS

Sanguinaria Canadensis

SANGUINARIA 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 Sanguinaria Canadensis Root.

Product ID15631-0389_8dc85a59-a6b0-413b-abe9-149640e7fb82
NDC15631-0389
Product TypeHuman Otc Drug
Proprietary NameSANGUINARIA CANADENSIS
Generic NameSanguinaria Canadensis
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 NameSANGUINARIA CANADENSIS ROOT
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0389-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0389-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0389-2 [15631038902]

SANGUINARIA CANADENSIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0389-0 [15631038900]

SANGUINARIA CANADENSIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0389-1 [15631038901]

SANGUINARIA CANADENSIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0389-4 [15631038904]

SANGUINARIA CANADENSIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0389-3 [15631038903]

SANGUINARIA CANADENSIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0389-5 [15631038905]

SANGUINARIA CANADENSIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

Drug Details

Active Ingredients

IngredientStrength
SANGUINARIA CANADENSIS ROOT1 [hp_X]/1

OpenFDA Data

SPL SET ID:a7493658-50de-4844-8dcb-47d147373f61
Manufacturer
UNII

NDC Crossover Matching brand name "SANGUINARIA CANADENSIS" or generic name "Sanguinaria Canadensis"

NDCBrand NameGeneric Name
0220-4481Sanguinaria canadensisSANGUINARIA CANADENSIS ROOT
0220-4482Sanguinaria canadensisSANGUINARIA CANADENSIS ROOT
0220-4483Sanguinaria canadensisSANGUINARIA CANADENSIS ROOT
0220-4484Sanguinaria canadensisSANGUINARIA CANADENSIS ROOT
0220-4485Sanguinaria canadensisSANGUINARIA CANADENSIS ROOT
0220-4486Sanguinaria canadensisSANGUINARIA CANADENSIS ROOT
0220-4487Sanguinaria canadensisSANGUINARIA CANADENSIS ROOT
0220-4550Sanguinaria canadensisSANGUINARIA CANADENSIS ROOT
0360-0350SANGUINARIA CANADENSISSANGUINARIA CAN
15631-0389SANGUINARIA CANADENSISSANGUINARIA CANADENSIS
15631-0679SANGUINARIA CANADENSISSANGUINARIA CANADENSIS
37662-2253Sanguinaria CanadensisSanguinaria Canadensis
37662-2254Sanguinaria CanadensisSanguinaria Canadensis
37662-2255Sanguinaria CanadensisSanguinaria Canadensis
37662-2256Sanguinaria CanadensisSanguinaria Canadensis
37662-2257Sanguinaria CanadensisSanguinaria Canadensis
37662-2258Sanguinaria CanadensisSanguinaria Canadensis
37662-2259Sanguinaria CanadensisSanguinaria Canadensis
37662-2260Sanguinaria CanadensisSanguinaria Canadensis
62106-8837SANGUINARIA CANADENSISBloodroot
68428-619Sanguinaria canadensisSANGUINARIA CANADENSIS ROOT
69152-1218Sanguinaria canadensis 200CSanguinaria canadensis

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.