NDC 48951-2119

Berberis Larix

Berberis Larix

Berberis Larix is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc. The primary component is Achillea Millefolium; Berberis Vulgaris Root Bark; Equisetum Arvense Top; Lytta Vesicatoria; Apis Mellifera; Larix Decidua Resin.

Product ID48951-2119_6d94f4d0-0a7a-b284-e053-2a91aa0ab707
NDC48951-2119
Product TypeHuman Otc Drug
Proprietary NameBerberis Larix
Generic NameBerberis Larix
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2009-09-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameUriel Pharmacy Inc
Substance NameACHILLEA MILLEFOLIUM; BERBERIS VULGARIS ROOT BARK; EQUISETUM ARVENSE TOP; LYTTA VESICATORIA; APIS MELLIFERA; LARIX DECIDUA RESIN
Active Ingredient Strength3 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 48951-2119-2

1350 PELLET in 1 BOTTLE, GLASS (48951-2119-2)
Marketing Start Date2009-09-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 48951-2119-2 [48951211902]

Berberis Larix PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01

Drug Details

Active Ingredients

IngredientStrength
ACHILLEA MILLEFOLIUM3 [hp_X]/1

OpenFDA Data

SPL SET ID:dcc3354c-e05b-11de-8a39-0800200c9a66
Manufacturer
UNII

NDC Crossover Matching brand name "Berberis Larix" or generic name "Berberis Larix"

NDCBrand NameGeneric Name
48951-2042Berberis LarixBerberis Larix
48951-2119Berberis LarixBerberis Larix

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