43857-0555 NDC - OSTEOPLEX (EQUISETUM HYEMALE, MAGNESIA MURIATICA, ASCORBICUM ACIDUM, MANGANUM MURIATICUM, SYMPHYTUM OFFICINALE, MEDULLA OSSIS SUIS, CALCAREA FLUORICA, CALCAREA PHOSPHORICA, SILICEA, PARATHYROID GLAND (SUIS), LIGAMENT (SUIS))

Drug Information

Product NDC: 43857-0555

Proprietary Name: Osteoplex

Non Proprietary Name: Equisetum Hyemale, Magnesia Muriatica, Ascorbicum Acidum, Manganum Muriaticum, Symphytum Officinale, Medulla Ossis Suis, Calcarea Fluorica, Calcarea Phosphorica, Silicea, Parathyroid Gland (Suis), Ligament (Suis)

Active Ingredient(s):
  • 3 [hp_X]/mL EQUISETUM HYEMALE WHOLE;
  • 3 [hp_X]/mL MAGNESIUM CHLORIDE;
  • 6 [hp_X]/mL ASCORBIC ACID;
  • 6 [hp_X]/mL MANGANESE CHLORIDE;
  • 6 [hp_X]/mL COMFREY ROOT;
  • 8 [hp_X]/mL SUS SCROFA BONE MARROW;
  • 12 [hp_X]/mL CALCIUM FLUORIDE;
  • 12 [hp_X]/mL TRIBASIC CALCIUM PHOSPHATE;
  • 12 1/mL SILICON DIOXIDE;
  • 8 [hp_C]/mL SUS SCROFA PARATHYROID GLAND;
  • 30 [hp_C]/mL SUS SCROFA LIGAMENT


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Labeler Information

Labeler Name: BioActive Nutritional, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:7/15/2020

Package Information

No. Package Code Package Description Billing Unit
143857-0555-130 mL in 1 BOTTLE, DROPPER (43857-0555-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43857-0555The 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 NAMEOsteoplexThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEEquisetum Hyemale, Magnesia Muriatica, Ascorbicum Acidum, Manganum Muriaticum, Symphytum Officinale, Medulla Ossis Suis, Calcarea Fluorica, Calcarea Phosphorica, Silicea, Parathyroid Gland (Suis), Ligament (Suis)The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe 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 DATE7/15/2020This 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 NAMEBioActive Nutritional, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEEQUISETUM HYEMALE WHOLE; MAGNESIUM CHLORIDE; ASCORBIC ACID; MANGANESE CHLORIDE; COMFREY ROOT; SUS SCROFA BONE MARROW; CALCIUM FLUORIDE; TRIBASIC CALCIUM PHOSPHATE; SILICON DIOXIDE; SUS SCROFA PARATHYROID GLAND; SUS SCROFA LIGAMENTThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH3; 3; 6; 6; 6; 8; 12; 12; 12; 8; 30 
ACTIVE INGRED UNIT[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; 1/mL; [hp_C]/mL; [hp_C]/mL 

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