NDC Package 69842-285-35 Sodium Chloride Hypertonicity

Sodium Chloride Ointment Ophthalmic - 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:
69842-285-35
Package Description:
1 TUBE in 1 CARTON / 3.5 g in 1 TUBE
Product Code:
Proprietary Name:
Sodium Chloride Hypertonicity
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:
69842028535
NDC to RxNorm Crosswalk:
  • RxCUI: 1298435 - sodium chloride 5 % Ophthalmic Ointment
  • RxCUI: 1298435 - sodium chloride 0.000855 MEQ/MG Ophthalmic Ointment
  • RxCUI: 1298435 - NaCl 0.000855 MEQ/MG Ophthalmic Ointment
  • RxCUI: 1298435 - NaCl 5 % Ophthalmic Ointment
  • RxCUI: 1298435 - sodium chloride 50 MG (5 % ) Ophthalmic Ointment
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Cvs Pharmacy
    Dosage Form:
    Ointment - A semisolid3 dosage form, usually containing <20% water and volatiles5 and >50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
    Administration Route(s):
  • Ophthalmic - Administration to the external eye.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    part349
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    05-01-2020
    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 69842-285-35?

    The NDC Packaged Code 69842-285-35 is assigned to a package of 1 tube in 1 carton / 3.5 g in 1 tube of Sodium Chloride Hypertonicity, a human over the counter drug labeled by Cvs Pharmacy. The product's dosage form is ointment and is administered via ophthalmic form.

    Is NDC 69842-285 included in the NDC Directory?

    Yes, Sodium Chloride Hypertonicity with product code 69842-285 is active and included in the NDC Directory. The product was first marketed by Cvs Pharmacy on May 01, 2020 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 69842-285-35?

    The 11-digit format is 69842028535. 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 5-3-2 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
    5-3-269842-285-355-4-269842-0285-35