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  5. NDC Package Code: 83027-0053-1 Bone Liquescence

NDC Package 83027-0053-1 Bone Liquescence

Taraxacum Officinale,Trifolium Pratense,Calcarea Muriatica,Equisetum Arvense,Juglans - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
83027-0053-1
Package Description:
120 mL in 1 BOTTLE, GLASS
Product Code:
83027-0053
Proprietary Name:
Bone Liquescence
Non-Proprietary Name:
Taraxacum Officinale, Trifolium Pratense, Calcarea Muriatica, Equisetum Arvense, Juglans Nigra, Sesame Oil, Calcarea Sulphurica, Hepar Suis, Kidney (suis), Medulla Ossis Suis, Menadione, Thyroidinum (bovine), Vitamin A, Vitamin D3, Calcarea Phosphorica, Calcarea Carbonica, Calcarea Fluorica, Manganum Metallicum, Niccolum Metallicum, Magnesium Metallicum
Substance Name:
Black Walnut Husk; Calcium Chloride; Calcium Fluoride; Calcium Sulfate Anhydrous; Cholecalciferol; Equisetum Arvense Top; Magnesium; Manganese; Menadione; Nickel; Oyster Shell Calcium Carbonate, Crude; Pork Kidney; Pork Liver; Sesame Oil; Sus Scrofa Bone Marrow; Taraxacum Officinale; Thyroid, Bovine; Tribasic Calcium Phosphate; Trifolium Pratense Flower; Vitamin A
Usage Information:
Adults 1 to 2 teaspoons one to two times daily. Children under twelve one half adult dosage. Consult a physician for use in children under 12 years of age.
11-Digit NDC Billing Format:
83027005301
Product Type:
Human Otc Drug
Labeler Name:
Nutritional Specialties, Inc.
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • BLACK WALNUT HUSK 4 [hp_X]/mL
  • CALCIUM CHLORIDE 4 [hp_X]/mL
  • CALCIUM FLUORIDE 12 [hp_X]/mL
  • CALCIUM SULFATE ANHYDROUS 5 [hp_X]/mL
  • CHOLECALCIFEROL 6 [hp_X]/mL
  • EQUISETUM ARVENSE TOP 4 [hp_X]/mL
  • MAGNESIUM 15 [hp_X]/mL
  • MANGANESE 12 [hp_X]/mL
  • MENADIONE 6 [hp_X]/mL
  • NICKEL 12 [hp_X]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 9 [hp_X]/mL
  • PORK KIDNEY 6 [hp_X]/mL
  • PORK LIVER 6 [hp_X]/mL
  • SESAME OIL 4 [hp_X]/mL
  • SUS SCROFA BONE MARROW 6 [hp_X]/mL
  • TARAXACUM OFFICINALE 3 [hp_X]/mL
  • THYROID, BOVINE 6 [hp_X]/mL
  • TRIBASIC CALCIUM PHOSPHATE 9 [hp_X]/mL
  • TRIFOLIUM PRATENSE FLOWER 3 [hp_X]/mL
  • VITAMIN A 6 [hp_X]/mL
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
  • Calcium - [CS]
  • Cations, Divalent - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Increased Coagulation Factor Activity - [PE] (Physiologic Effect)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Phosphate Binder - [EPC] (Established Pharmacologic Class)
  • Phosphate Chelating Activity - [MoA] (Mechanism of Action)
  • Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
  • Vitamin A - [CS]
  • Vitamin A - [EPC] (Established Pharmacologic Class)
  • Vitamin D - [CS]
  • Vitamin D - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    05-17-2023
    End Marketing Date:
    05-25-2028
    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.

    Frequently Asked Questions

    What is NDC 83027-0053-1?

    The NDC Packaged Code 83027-0053-1 is assigned to a package of 120 ml in 1 bottle, glass of Bone Liquescence, a human over the counter drug labeled by Nutritional Specialties, Inc.. The product's dosage form is liquid and is administered via oral form.

    Is NDC 83027-0053 included in the NDC Directory?

    Yes, Bone Liquescence with product code 83027-0053 is active and included in the NDC Directory. The product was first marketed by Nutritional Specialties, Inc. on May 17, 2023.

    What is the 11-digit format for NDC 83027-0053-1?

    The 11-digit format is 83027005301. 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
    5-4-183027-0053-15-4-283027-0053-01