NDC 15631-0377

RUMEX ACETOSA

Rumex Acetosa

RUMEX ACETOSA 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 Rumex Acetosa Leaf.

Product ID15631-0377_3f78546a-e6e7-4533-94e7-a09aca731ede
NDC15631-0377
Product TypeHuman Otc Drug
Proprietary NameRUMEX ACETOSA
Generic NameRumex Acetosa
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-29
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameRUMEX ACETOSA LEAF
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0377-0

100 PELLET in 1 PACKAGE (15631-0377-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0377-0 [15631037700]

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

NDC 15631-0377-3 [15631037703]

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

NDC 15631-0377-4 [15631037704]

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

NDC 15631-0377-1 [15631037701]

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

NDC 15631-0377-2 [15631037702]

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

NDC 15631-0377-5 [15631037705]

RUMEX ACETOSA 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
RUMEX ACETOSA LEAF1 [hp_X]/1

OpenFDA Data

SPL SET ID:1c04b801-27fa-46b4-8fad-60dc1b445529
Manufacturer
UNII

NDC Crossover Matching brand name "RUMEX ACETOSA" or generic name "Rumex Acetosa"

NDCBrand NameGeneric Name
15631-0377RUMEX ACETOSARUMEX ACETOSA
68428-607Rumex acetosaRUMEX ACETOSA LEAF
71919-592Rumex acetosaRUMEX ACETOSA LEAF

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