17089-259 NDC - OSTEOBIOS (CALCITONIN HUMAN - CALCIUM CARBONATE - CALCIUM FLUORIDE - CALCIUM PHOSPHATE - ISOLEUCINE - LEUCINE - LYSINE - METHIONINE - PHENYLALANINE - SUS SCROFA BONE - SUS SCROFA PARATHYROID GLAND - THREONINE - TRYPTOPHAN - VALINE -)

Drug Information

Product NDC: 17089-259

Proprietary Name: OSTEOBIOS

Non Proprietary Name: CALCITONIN HUMAN - CALCIUM CARBONATE - CALCIUM FLUORIDE - CALCIUM PHOSPHATE - ISOLEUCINE - LEUCINE - LYSINE - METHIONINE - PHENYLALANINE - SUS SCROFA BONE - SUS SCROFA PARATHYROID GLAND - THREONINE - TRYPTOPHAN - VALINE -

Active Ingredient(s):
  • 6 [hp_X]/30mL CALCITONIN HUMAN;
  • 3 [hp_X]/30mL ISOLEUCINE;
  • 3 [hp_X]/30mL LEUCINE;
  • 3 [hp_X]/30mL LYSINE;
  • 3 [hp_X]/30mL METHIONINE;
  • 3 [hp_X]/30mL PHENYLALANINE;
  • 3 [hp_X]/30mL THREONINE;
  • 3 [hp_X]/30mL TRYPTOPHAN;
  • 3 [hp_X]/30mL VALINE;
  • 30 [hp_X]/30mL CALCIUM CARBONATE;
  • 30 [hp_X]/30mL CALCIUM FLUORIDE;
  • 30 [hp_X]/30mL CALCIUM PHOSPHATE;
  • 30 [hp_X]/30mL SUS SCROFA BONE;
  • 30 [hp_X]/30mL SUS SCROFA PARATHYROID GLAND


Administration Route(s): ORAL

Dosage Form(s): SOLUTION/ DROPS

Labeler Information

Labeler Name: Guna spa
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:5/23/2006

Package Information

No. Package Code Package Description Billing Unit
117089-259-181 BOTTLE, DROPPER in 1 BOX (17089-259-18) > 30 mL in 1 BOTTLE, DROPPER

NDC Record

Field Name Field Value Definition
PRODUCT NDC17089-259The 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 NAMEOSTEOBIOSThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMECALCITONIN HUMAN - CALCIUM CARBONATE - CALCIUM FLUORIDE - CALCIUM PHOSPHATE - ISOLEUCINE - LEUCINE - LYSINE - METHIONINE - PHENYLALANINE - SUS SCROFA BONE - SUS SCROFA PARATHYROID GLAND - THREONINE - TRYPTOPHAN - VALINE -The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESOLUTION/ DROPSThe 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 DATE5/23/2006This 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 NAMEGuna spaName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMECALCITONIN HUMAN; ISOLEUCINE; LEUCINE; LYSINE; METHIONINE; PHENYLALANINE; THREONINE; TRYPTOPHAN; VALINE; CALCIUM CARBONATE; CALCIUM FLUORIDE; CALCIUM PHOSPHATE; SUS SCROFA BONE; SUS SCROFA PARATHYROID GLANDThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH6; 3; 3; 3; 3; 3; 3; 3; 3; 30; 30; 30; 30; 30 
ACTIVE INGRED UNIT[hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL 

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This page was last updated on: 8/16/2021