NDC 15631-0518

ARALIA RACEMOSA

Aralia Racemosa

ARALIA RACEMOSA is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc. The primary component is Aralia Racemosa Root.

Product ID15631-0518_090fabb8-cbc5-4173-9e8c-1ff81de2764e
NDC15631-0518
Product TypeHuman Otc Drug
Proprietary NameARALIA RACEMOSA
Generic NameAralia Racemosa
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-12-18
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameARALIA RACEMOSA ROOT
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0518-6

1000 TABLET in 1 CONTAINER (15631-0518-6)
Marketing Start Date2015-12-18
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0518-0 [15631051800]

ARALIA RACEMOSA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-18
Inactivation Date2020-01-31

NDC 15631-0518-1 [15631051801]

ARALIA RACEMOSA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-18
Inactivation Date2020-01-31

NDC 15631-0518-6 [15631051806]

ARALIA RACEMOSA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-18
Inactivation Date2020-01-31

NDC 15631-0518-4 [15631051804]

ARALIA RACEMOSA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-18
Inactivation Date2020-01-31

NDC 15631-0518-2 [15631051802]

ARALIA RACEMOSA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-18
Inactivation Date2020-01-31

NDC 15631-0518-7 [15631051807]

ARALIA RACEMOSA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-18
Inactivation Date2020-01-31

NDC 15631-0518-5 [15631051805]

ARALIA RACEMOSA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-18
Inactivation Date2020-01-31

NDC 15631-0518-3 [15631051803]

ARALIA RACEMOSA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-18
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ARALIA RACEMOSA ROOT1 [hp_X]/1

OpenFDA Data

SPL SET ID:863583a1-782d-45aa-8adf-b5ea6c7cd7bf
Manufacturer
UNII
UPC Code
  • 8907460005526
  • NDC Crossover Matching brand name "ARALIA RACEMOSA" or generic name "Aralia Racemosa"

    NDCBrand NameGeneric Name
    0220-0442Aralia racemosaARALIA RACEMOSA ROOT
    0220-0444Aralia racemosaARALIA RACEMOSA ROOT
    15631-0042ARALIA RACEMOSAARALIA RACEMOSA
    15631-0518ARALIA RACEMOSAARALIA RACEMOSA
    63545-080Aralia RacemosaAralia Racemosa
    63545-081Aralia RacemosaAralia Racemosa
    63545-082Aralia RacemosaAralia Racemosa
    63545-083Aralia RacemosaAralia Racemosa
    63545-084Aralia RacemosaAralia Racemosa
    63545-085Aralia RacemosaAralia Racemosa
    63545-086Aralia RacemosaAralia Racemosa
    68428-218Aralia racemosaARALIA RACEMOSA ROOT
    71919-073Aralia racemosaARALIA RACEMOSA ROOT
    66096-751Aralia Racemosa MTAralia Racemosa

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