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  5. NDC Package Code: 58264-0135-1 D-129

NDC Package 58264-0135-1 D-129

Sodium Chloride Solution Sublingual - 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:
58264-0135-1
Package Description:
29.57 mL in 1 BOTTLE, GLASS
Product Code:
58264-0135
Proprietary Name:
D-129
Non-Proprietary Name:
Sodium Chloride
Substance Name:
Sodium Chloride
Usage Information:
This product is used to treat dryness inside the nose (nasal passages). It helps add moisture inside the nose to dissolve and soften thick or crusty mucus. In babies and young children with stuffy noses who cannot blow their noses, using this product helps to make the mucus easier to remove with a nasal bulb syringe. This helps relieve stuffiness and makes breathing easier. This product contains a purified gentle salt solution (also called saline or sodium chloride solution). It does not contain any medication.
11-Digit NDC Billing Format:
58264013501
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.
    • Active Ingredient(s):
  • SODIUM CHLORIDE 6 [hp_X]/mL
    • 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 58264-0135-1?

    The NDC Packaged Code 58264-0135-1 is assigned to a package of 29.57 ml in 1 bottle, glass of D-129, 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 58264-0135 included in the NDC Directory?

    Yes, D-129 with product code 58264-0135 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 58264-0135-1?

    The 11-digit format is 58264013501. 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
    5-4-158264-0135-15-4-258264-0135-01