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  5. NDC Package Code: 54973-1068-2 Bioplasma

NDC Package 54973-1068-2 Bioplasma

Calcium Fluoride,Tribasic Calcium Phosphate,Calcium Sulfate Anhydrous,Ferrosoferric - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
54973-1068-2
Package Description:
1000 TABLET, SOLUBLE in 1 BOTTLE, PLASTIC
Product Code:
54973-1068
Proprietary Name:
Bioplasma
Non-Proprietary Name:
Calcium Fluoride, Tribasic Calcium Phosphate, Calcium Sulfate Anhydrous, Ferrosoferric Phosphate, Potassium Chloride, Potassium Phosphate, Dibasic, Potassium Sulfate, Magnesium Phosphate, Dibasic Trihydrate, Sodium Chloride, Sodium Phosphate, Dibasic, Heptahydrate, Sodium Sulfate, And Silicon Dioxide
Substance Name:
Calcium Fluoride; Calcium Sulfate Anhydrous; Ferrosoferric Phosphate; Magnesium Phosphate, Dibasic Trihydrate; Potassium Chloride; Potassium Phosphate, Dibasic; Potassium Sulfate; Silicon Dioxide; Sodium Chloride; Sodium Phosphate, Dibasic, Heptahydrate; Sodium Sulfate; Tribasic Calcium Phosphate
Usage Information:
For relief of symptoms of colds, simple nervous tension, fatigue and headaches.
11-Digit NDC Billing Format:
54973106802
Product Type:
Human Otc Drug
Labeler Name:
Hyland's Inc.
Dosage Form:
Tablet, Soluble - A solid dosage form that contains medicinal substances with or without suitable diluents and possesses the ability to dissolve in fluids.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • CALCIUM FLUORIDE 6 [hp_X]/1
  • CALCIUM SULFATE ANHYDROUS 3 [hp_X]/1
  • FERROSOFERRIC PHOSPHATE 3 [hp_X]/1
  • MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 3 [hp_X]/1
  • POTASSIUM CHLORIDE 3 [hp_X]/1
  • POTASSIUM PHOSPHATE, DIBASIC 3 [hp_X]/1
  • POTASSIUM SULFATE 3 [hp_X]/1
  • SILICON DIOXIDE 6 [hp_X]/1
  • SODIUM CHLORIDE 6 [hp_X]/1
  • SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE 3 [hp_X]/1
  • SODIUM SULFATE 3 [hp_X]/1
  • TRIBASIC CALCIUM PHOSPHATE 3 [hp_X]/1
    • Pharmacologic Class(es):
  • Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
  • Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
  • Calcium - [CS]
  • Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
  • Cations, Divalent - [CS]
  • Increased Coagulation Factor Activity - [PE] (Physiologic Effect)
  • Increased Large Intestinal Motility - [PE] (Physiologic Effect)
  • Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Inhibition Small Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Magnesium Ion Exchange Activity - [MoA] (Mechanism of Action)
  • Osmotic Activity - [MoA] (Mechanism of Action)
  • Osmotic Laxative - [EPC] (Established Pharmacologic Class)
  • Potassium Compounds - [CS]
  • Potassium Salt - [EPC] (Established Pharmacologic Class)
  • Stimulation Large Intestine Fluid/Electrolyte Secretion - [PE] (Physiologic Effect)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    01-01-1940
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    54973-1068-1500 TABLET, SOLUBLE in 1 BOTTLE, PLASTIC

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 54973-1068-2?

    The NDC Packaged Code 54973-1068-2 is assigned to a package of 1000 tablet, soluble in 1 bottle, plastic of Bioplasma, a human over the counter drug labeled by Hyland's Inc.. The product's dosage form is tablet, soluble and is administered via oral form.

    Is NDC 54973-1068 included in the NDC Directory?

    Yes, Bioplasma with product code 54973-1068 is active and included in the NDC Directory. The product was first marketed by Hyland's Inc. on January 01, 1940 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 54973-1068-2?

    The 11-digit format is 54973106802. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-4-154973-1068-25-4-254973-1068-02