48951-2157 NDC - BERBERIS LARIX

Drug Information

  • Product NDC: 48951-2157
  • Proprietary Name: Berberis Larix
  • Non Proprietary Name: Berberis Larix
  • Active Ingredient(s): 3 [hp_X]/1 ACHILLEA MILLEFOLIUM; 8 [hp_X]/1 APIS MELLIFERA; 3 [hp_X]/1 BERBERIS VULGARIS ROOT BARK; 3 [hp_X]/1 EQUISETUM ARVENSE TOP; 8 [hp_X]/1 FERROUS DISULFIDE; 8 [hp_X]/1 LARIX DECIDUA RESIN; 6 [hp_X]/1 LYTTA VESICATORIA; 8 [hp_X]/1 SUS SCROFA URINARY BLADDER
  • Administration Route(s): ORAL
  • Dosage Form(s): PELLET
  • Pharmacy Class(es): Allergens [CS]; Bee Venoms [CS]; Cell-mediated Immunity [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Standardized Insect Venom Allergenic Extract [EPC]

Labeler Information

Field Name Field Value
Labeler Name: Uriel Pharmacy Inc
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:9/1/2009

Package Information

No. Package Code Package Description Billing Unit
148951-2157-21350 PELLET in 1 BOTTLE, GLASS (48951-2157-2)

NDC Record

Field Name Field Value Definition
PRODUCT NDC48951-2157The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEBerberis LarixThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEBerberis LarixThe translation of the dosage form Code submitted by the firm.
DOSAGE FORM NAMEPELLETThis is the date that the labeler indicates was the start of its marketing of the drug product.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE9/1/2009This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMEUriel Pharmacy IncThis corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
SUBSTANCE NAMEACHILLEA MILLEFOLIUM; APIS MELLIFERA; BERBERIS VULGARIS ROOT BARK; EQUISETUM ARVENSE TOP; FERROUS DISULFIDE; LARIX DECIDUA RESIN; LYTTA VESICATORIA; SUS SCROFA URINARY BLADDERName of Company corresponding to the labeler code segment of the Product NDC.
ACTIVE NUMERATOR STRENGTH3; 8; 3; 3; 8; 8; 6; 8 
ACTIVE INGRED UNIT[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 
PHARM CLASSESAllergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC] 

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This page was last updated on: 12/19/2025

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