NDC 71919-657

SUMBUL

Ferula Sumbul

SUMBUL is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Washington Homeopathic Products. The primary component is Ferula Sumbul Root.

Product ID71919-657_99b7dd29-ee89-7231-e053-2995a90a93f9
NDC71919-657
Product TypeHuman Otc Drug
Proprietary NameSUMBUL
Generic NameFerula Sumbul
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2011-05-17
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameWashington Homeopathic Products
Substance NameFERULA SUMBUL ROOT
Active Ingredient Strength30 [hp_C]/mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 71919-657-07

15 mL in 1 VIAL, GLASS (71919-657-07)
Marketing Start Date2011-05-17
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71919-657-07 [71919065707]

SUMBUL LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-05-17

NDC 71919-657-08 [71919065708]

SUMBUL LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-05-17

NDC 71919-657-09 [71919065709]

SUMBUL LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-05-17

NDC 71919-657-10 [71919065710]

SUMBUL LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-05-17

Drug Details

Active Ingredients

IngredientStrength
FERULA SUMBUL ROOT30 [hp_C]/mL

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

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

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