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48951-2135 NDC - BAMBUSA ARGENTUM

Drug Information

Product NDC: 48951-2135

Proprietary Name: Bambusa Argentum

Non Proprietary Name: Bambusa Argentum

Active Ingredient(s):
  • 22 [hp_X]/g ARNICA MONTANA;
  • 8 [hp_X]/g BAMBUSA VULGARIS WHOLE;
  • 10 [hp_X]/g BOS TAURUS INTERVERTEBRAL DISC;
  • 9 [hp_X]/g FORMICA RUFA;
  • 8 [hp_X]/g ROSMARINUS OFFICINALIS FLOWERING TOP;
  • 19 [hp_X]/g SILICON DIOXIDE;
  • 22 [hp_X]/g SILVER;
  • 8 [hp_X]/g STACHYS OFFICINALIS;
  • 4 [hp_X]/g VISCUM ALBUM FRUITING TOP


Administration Route(s): RECTAL

Dosage Form(s): SUPPOSITORY

Labeler Information

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
148951-2135-110 BLISTER PACK in 1 BOX (48951-2135-1) / 2 g in 1 BLISTER PACK

NDC Record

Field Name Field Value Definition
PRODUCT NDC48951-2135The 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 NAMEBambusa ArgentumThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEBambusa ArgentumThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESUPPOSITORYThe translation of the dosage form Code submitted by the firm.
ROUTE NAMERECTALThe 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 Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEARNICA MONTANA; BAMBUSA VULGARIS WHOLE; BOS TAURUS INTERVERTEBRAL DISC; FORMICA RUFA; ROSMARINUS OFFICINALIS FLOWERING TOP; SILICON DIOXIDE; SILVER; STACHYS OFFICINALIS; VISCUM ALBUM FRUITING TOPAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH22; 8; 10; 9; 8; 19; 22; 8; 4 
ACTIVE INGRED UNIT[hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g 

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This page was last updated on: 2/1/2023