NDC 15631-0018

ALOE SOCOTRINA

Aloe Socotrina

ALOE SOCOTRINA 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 Aloe.

Product ID15631-0018_04888900-b9a9-4c89-84b7-5edb40683f20
NDC15631-0018
Product TypeHuman Otc Drug
Proprietary NameALOE SOCOTRINA
Generic NameAloe Socotrina
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 NameALOE
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0018-0

100 PELLET in 1 PACKAGE (15631-0018-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0018-5 [15631001805]

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

NDC 15631-0018-3 [15631001803]

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

NDC 15631-0018-1 [15631001801]

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

NDC 15631-0018-2 [15631001802]

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

NDC 15631-0018-0 [15631001800]

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

NDC 15631-0018-4 [15631001804]

ALOE SOCOTRINA 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
ALOE1 [hp_X]/1

OpenFDA Data

SPL SET ID:9294683e-beaa-4c58-9b08-9890f1b61e43
Manufacturer
UNII

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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