NDC 15631-0017

ALNUS GLUTINOSA

Alnus Glutinosa

ALNUS GLUTINOSA 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 Alnus Glutinosa Bark.

Product ID15631-0017_9e45eedb-9ee2-4f4e-e053-2995a90a26fc
NDC15631-0017
Product TypeHuman Otc Drug
Proprietary NameALNUS GLUTINOSA
Generic NameAlnus Glutinosa
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 NameALNUS GLUTINOSA BARK
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0017-0

100 PELLET in 1 PACKAGE (15631-0017-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0017-5 [15631001705]

ALNUS GLUTINOSA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-11

NDC 15631-0017-4 [15631001704]

ALNUS GLUTINOSA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-11

NDC 15631-0017-1 [15631001701]

ALNUS GLUTINOSA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-11

NDC 15631-0017-3 [15631001703]

ALNUS GLUTINOSA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-11

NDC 15631-0017-0 [15631001700]

ALNUS GLUTINOSA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-11

NDC 15631-0017-2 [15631001702]

ALNUS GLUTINOSA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-11

Drug Details

Active Ingredients

IngredientStrength
ALNUS GLUTINOSA BARK1 [hp_X]/1

OpenFDA Data

SPL SET ID:2d4a081d-1f05-4b15-96ea-63ab88d6e07a
Manufacturer
UNII

NDC Crossover Matching brand name "ALNUS GLUTINOSA" or generic name "Alnus Glutinosa"

NDCBrand NameGeneric Name
15631-0017ALNUS GLUTINOSAALNUS GLUTINOSA
60512-6473ALNUS GLUTINOSAALNUS GLUTINOSA

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