NDC 15631-0267

LAPPA MAJOR

Lappa Major

LAPPA MAJOR 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 Arctium Lappa Root.

Product ID15631-0267_8e61d79b-ba15-4cc0-a988-be2001003483
NDC15631-0267
Product TypeHuman Otc Drug
Proprietary NameLAPPA MAJOR
Generic NameLappa Major
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-05
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameARCTIUM LAPPA ROOT
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0267-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0267-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0267-0 [15631026700]

LAPPA MAJOR PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0267-1 [15631026701]

LAPPA MAJOR PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0267-2 [15631026702]

LAPPA MAJOR PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0267-4 [15631026704]

LAPPA MAJOR PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0267-5 [15631026705]

LAPPA MAJOR PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0267-3 [15631026703]

LAPPA MAJOR PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

Drug Details

Active Ingredients

IngredientStrength
ARCTIUM LAPPA ROOT1 [hp_X]/1

OpenFDA Data

SPL SET ID:ad7db0ab-fd18-405f-96b2-02079e7b9e45
Manufacturer
UNII

NDC Crossover Matching brand name "LAPPA MAJOR" or generic name "Lappa Major"

NDCBrand NameGeneric Name
15631-0267LAPPA MAJORLAPPA MAJOR
68428-469Lappa majorARCTIUM LAPPA ROOT
71919-404Lappa majorARCTIUM LAPPA ROOT

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