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Drug Information

Product NDC: 48951-8234

Proprietary Name: Periodontium Quartz Special Order

Non Proprietary Name: Periodontium Quartz Special Order

Active Ingredient(s):
  • 17 [hp_X]/1 ATROPA BELLADONNA;
  • 17 [hp_X]/1 BEEF TONGUE;
  • 17 [hp_X]/1 BOS TAURUS BONE;
  • 30 [hp_X]/1 SILICON DIOXIDE;
  • 20 [hp_X]/1 SILVER;
  • 17 [hp_X]/1 SUS SCROFA TOOTH

Administration Route(s): ORAL

Dosage Form(s): PELLET

Labeler Information

Labeler Name: Uriel Pharmacy Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Start Marketing Date:9/1/2009

Package Information

No. Package Code Package Description Billing Unit
148951-8234-21350 PELLET in 1 BOTTLE, GLASS (48951-8234-2)

NDC Record

Field Name Field Value Definition
PRODUCT NDC48951-8234The 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 NAMEPeriodontium Quartz Special OrderThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEPeriodontium Quartz Special OrderThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEPELLETThe translation of the dosage form Code submitted by the firm.
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 under Structured Product Labeling Resources.
LABELER NAMEUriel Pharmacy Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEATROPA BELLADONNA; BEEF TONGUE; BOS TAURUS BONE; CALENDULA OFFICINALIS FLOWERING TOP; SILICON DIOXIDE; SILVER; SUS SCROFA TOOTHAn 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 STRENGTH17; 17; 17; 3; 30; 20; 17 
ACTIVE INGRED UNIT[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 

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