NDC 71919-446

Melilotus alba

Melilotus Albus Top

Melilotus alba is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Washington Homeopathic Products. The primary component is Melilotus Albus Top.

Product ID71919-446_7e57b220-8a21-7266-e053-2991aa0a025a
NDC71919-446
Product TypeHuman Otc Drug
Proprietary NameMelilotus alba
Generic NameMelilotus Albus Top
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2010-02-03
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameWashington Homeopathic Products
Substance NameMELILOTUS ALBUS TOP
Active Ingredient Strength30 [hp_C]/mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 71919-446-07

15 mL in 1 VIAL, GLASS (71919-446-07)
Marketing Start Date2010-02-03
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71919-446-07 [71919044607]

Melilotus alba LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-03

NDC 71919-446-10 [71919044610]

Melilotus alba LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-03

NDC 71919-446-08 [71919044608]

Melilotus alba LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-03

NDC 71919-446-09 [71919044609]

Melilotus alba LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-03

Drug Details

Active Ingredients

IngredientStrength
MELILOTUS ALBUS TOP30 [hp_C]/mL

OpenFDA Data

SPL SET ID:71a87b69-2bda-473e-8265-ab2e9316b2b9
Manufacturer
UNII
UPC Code
  • 0740640382769
  • NDC Crossover Matching brand name "Melilotus alba" or generic name "Melilotus Albus Top"

    NDCBrand NameGeneric Name
    68428-496Melilotus albaMELILOTUS OFFICINALIS TOP
    71919-446Melilotus albaMELILOTUS ALBUS TOP

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