NDC 15631-0509

ALOE SOCOTRINA

Aloe Socotrina

ALOE SOCOTRINA 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 Aloe.

Product ID15631-0509_00c9c670-2a64-4f9a-b47e-6762d9f9e97d
NDC15631-0509
Product TypeHuman Otc Drug
Proprietary NameALOE SOCOTRINA
Generic NameAloe Socotrina
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-12-07
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameALOE
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0509-6

1000 TABLET in 1 CONTAINER (15631-0509-6)
Marketing Start Date2015-12-07
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0509-7 [15631050907]

ALOE SOCOTRINA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-07
Inactivation Date2020-01-31

NDC 15631-0509-5 [15631050905]

ALOE SOCOTRINA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-07
Inactivation Date2020-01-31

NDC 15631-0509-2 [15631050902]

ALOE SOCOTRINA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-07
Inactivation Date2020-01-31

NDC 15631-0509-6 [15631050906]

ALOE SOCOTRINA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-07
Inactivation Date2020-01-31

NDC 15631-0509-1 [15631050901]

ALOE SOCOTRINA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-07
Inactivation Date2020-01-31

NDC 15631-0509-0 [15631050900]

ALOE SOCOTRINA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-07
Inactivation Date2020-01-31

NDC 15631-0509-3 [15631050903]

ALOE SOCOTRINA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-07
Inactivation Date2020-01-31

NDC 15631-0509-4 [15631050904]

ALOE SOCOTRINA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-07
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ALOE1 [hp_X]/1

OpenFDA Data

SPL SET ID:73dceba6-29ae-470b-b46d-6e208ce3cab2
Manufacturer
UNII
UPC Code
  • 8907460005526

    • NDC Crossover Matching brand name "ALOE SOCOTRINA" or generic name "Aloe Socotrina"

    NDCBrand NameGeneric Name
    15631-0018ALOE SOCOTRINAALOE SOCOTRINA
    15631-0509ALOE SOCOTRINAALOE SOCOTRINA
    63545-147Aloe socotrinaAloe socotrina
    63545-812Aloe socotrinaAloe socotrina
    63545-813Aloe socotrinaAloe socotrina
    63545-814Aloe socotrinaAloe socotrina
    63545-815Aloe socotrinaAloe socotrina
    63545-816Aloe socotrinaAloe socotrina
    63545-817Aloe socotrinaAloe socotrina
    63545-818Aloe socotrinaAloe socotrina
    63545-819Aloe socotrinaAloe socotrina
    68428-190Aloe SocotrinaALOE
    71919-031Aloe socotrinaALOE
    69152-1077Aloe socotrina 200CAloe socotrina
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