NDC 69152-1077

Aloe socotrina 200C

Aloe Socotrina

Aloe socotrina 200C is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Paramesh Banerji Life Sciences Llc. The primary component is Aloe.

Product ID69152-1077_39b64712-7a26-1903-e054-00144ff88e88
NDC69152-1077
Product TypeHuman Otc Drug
Proprietary NameAloe socotrina 200C
Generic NameAloe Socotrina
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-06-03
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameParamesh Banerji Life Sciences LLC
Substance NameALOE
Active Ingredient Strength200 [hp_C]/1
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 69152-1077-1

96 PELLET in 1 BOTTLE (69152-1077-1)
Marketing Start Date2015-06-03
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 69152-1077-1 [69152107701]

Aloe socotrina 200C PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-06-03
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ALOE200 [hp_C]/1

OpenFDA Data

SPL SET ID:179a83ee-ead4-5734-e054-00144ff8d46c
Manufacturer
UNII

NDC Crossover Matching brand name "Aloe socotrina 200C" or generic name "Aloe Socotrina"

NDCBrand NameGeneric Name
69152-1077Aloe socotrina 200CAloe socotrina
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
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.