NDC Package 58264-0212-1 N-14

Fucus Vesiculosus,Sodium Chloride,Lycopus Virginicus,Spongia Officinalis - View Billable Units, 11-Digit Format, RxNorm

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:
58264-0212-1
Package Description:
29.57 mL in 1 BOTTLE, GLASS
Product Code:
Proprietary Name:
N-14
Non-Proprietary Name:
Fucus Vesiculosus, Sodium Chloride, Lycopus Virginicus, Spongia Officinalis Skeleton, Roasted, Potassium Iodide, Calcium Iodide, Thyroid, Unspecified, Bos Taurus Adrenal Gland, Bos Taurus Pituitary Gland, Posterior, Bos Taurus Thymus, And Sus Scrofa Spleen
Substance Name:
Bos Taurus Adrenal Gland; Bos Taurus Pituitary Gland, Posterior; Bos Taurus Thymus; Calcium Iodide; Fucus Vesiculosus; Lycopus Virginicus; Potassium Iodide; Sodium Chloride; Spongia Officinalis Skeleton, Roasted; Sus Scrofa Spleen; Thyroid, Unspecified
Usage Information:
This product is used as Support for the Thyroid gland.
11-Digit NDC Billing Format:
58264021201
Product Type:
Human Otc Drug
Labeler Name:
Dna Labs, Inc.
Dosage Form:
Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Administration Route(s):
  • Sublingual - Administration beneath the tongue.
  • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    01-01-1990
    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.

    Frequently Asked Questions

    What is NDC 58264-0212-1?

    The NDC Packaged Code 58264-0212-1 is assigned to a package of 29.57 ml in 1 bottle, glass of N-14, a human over the counter drug labeled by Dna Labs, Inc.. The product's dosage form is solution and is administered via sublingual form.

    Is NDC 58264-0212 included in the NDC Directory?

    Yes, N-14 with product code 58264-0212 is active and included in the NDC Directory. The product was first marketed by Dna Labs, Inc. on January 01, 1990 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 58264-0212-1?

    The 11-digit format is 58264021201. 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
    5-4-158264-0212-15-4-258264-0212-01