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  5. NDC Package Code: 43014-1113-1 Resp Ease

NDC Package 43014-1113-1 Resp Ease

Sodium Chloride Liquid Nasal - 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:
43014-1113-1
Package Description:
25 VIAL in 1 CARTON / 5 mL in 1 VIAL
Product Code:
43014-1113
Proprietary Name:
Resp Ease
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:
43014111301
Product Type:
Human Otc Drug
Labeler Name:
Laboratoire Unither
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):
Nasal - Administration to the nose; administered by way of the nose.
Active Ingredient(s):
SODIUM CHLORIDE 60 mg/mL
Sample Package:
No
Marketing Category:
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date:
04-01-2025
Listing Expiration Date:
12-31-2026
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 43014-1113-1?

The NDC Packaged Code 43014-1113-1 is assigned to a package of 25 vial in 1 carton / 5 ml in 1 vial of Resp Ease, a human over the counter drug labeled by Laboratoire Unither. The product's dosage form is liquid and is administered via nasal form.

Is NDC 43014-1113 included in the NDC Directory?

Yes, Resp Ease with product code 43014-1113 is active and included in the NDC Directory. The product was first marketed by Laboratoire Unither on April 01, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 43014-1113-1?

The 11-digit format is 43014111301. 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
5-4-143014-1113-15-4-243014-1113-01