NDC 15631-0423

SUMBUL

Sumbul

SUMBUL 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 Ferula Sumbul Root.

Product ID15631-0423_a1c3d04c-3b02-58bf-e053-2a95a90a7638
NDC15631-0423
Product TypeHuman Otc Drug
Proprietary NameSUMBUL
Generic NameSumbul
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-11-03
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameFERULA SUMBUL ROOT
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0423-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0423-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0423-4 [15631042304]

SUMBUL PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0423-2 [15631042302]

SUMBUL PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0423-1 [15631042301]

SUMBUL PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0423-3 [15631042303]

SUMBUL PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0423-5 [15631042305]

SUMBUL PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0423-0 [15631042300]

SUMBUL PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

Drug Details

Active Ingredients

IngredientStrength
FERULA SUMBUL ROOT1 [hp_X]/1

OpenFDA Data

SPL SET ID:d51290bc-bb96-4cc1-89b6-1400b47a150b
Manufacturer
UNII

NDC Crossover Matching brand name "SUMBUL" or generic name "Sumbul"

NDCBrand NameGeneric Name
15631-0423SUMBULSUMBUL
68428-658SumbulFERULA SUMBUL ROOT
71919-657SUMBULFerula sumbul

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