NDC 15631-0021

ALUMEN

Alumen

ALUMEN 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 Potassium Alum.

Product ID15631-0021_9e49ea80-9e27-3f33-e053-2995a90aff3b
NDC15631-0021
Product TypeHuman Otc Drug
Proprietary NameALUMEN
Generic NameAlumen
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 NamePOTASSIUM ALUM
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0021-0

100 PELLET in 1 PACKAGE (15631-0021-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0021-4 [15631002104]

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

NDC 15631-0021-3 [15631002103]

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

NDC 15631-0021-0 [15631002100]

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

NDC 15631-0021-1 [15631002101]

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

NDC 15631-0021-2 [15631002102]

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

NDC 15631-0021-5 [15631002105]

ALUMEN 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
POTASSIUM ALUM3 [hp_X]/1

OpenFDA Data

SPL SET ID:d794dbdf-af8f-446c-b5d8-3b2f085d21fd
Manufacturer
UNII

NDC Crossover Matching brand name "ALUMEN" or generic name "Alumen"

NDCBrand NameGeneric Name
0220-0201AlumenPOTASSIUM ALUM
15631-0021ALUMENALUMEN
60512-6162ALUMENALUMEN
62106-4820ALUMENAluminum potassium sulfate
68428-192AlumenPOTASSIUM ALUM
71919-033AlumenPOTASSIUM ALUM

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