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  5. NDC Package Code: 69396-116-05 Saline Ampoules

NDC Package 69396-116-05 Saline Ampoules

Sodium Chloride 0.9% Spray Topical - 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:
69396-116-05
Package Description:
60 VIAL in 1 CARTON / 5 mL in 1 VIAL
Product Code:
69396-116
Proprietary Name:
Saline Ampoules
Non-Proprietary Name:
Sodium Chloride 0.9%
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:
69396011605
Product Type:
Human Otc Drug
Labeler Name:
Trifecta Pharmaceuticals Usa, Llc.
Dosage Form:
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route(s):
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s):
SODIUM CHLORIDE 9 mg/mL
Sample Package:
No
FDA Application Number:
M012
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
07-28-2022
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 69396-116-05?

The NDC Packaged Code 69396-116-05 is assigned to a package of 60 vial in 1 carton / 5 ml in 1 vial of Saline Ampoules, a human over the counter drug labeled by Trifecta Pharmaceuticals Usa, Llc.. The product's dosage form is spray and is administered via topical form.

Is NDC 69396-116 included in the NDC Directory?

Yes, Saline Ampoules with product code 69396-116 is active and included in the NDC Directory. The product was first marketed by Trifecta Pharmaceuticals Usa, Llc. on July 28, 2022 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 69396-116-05?

The 11-digit format is 69396011605. 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
5-3-269396-116-055-4-269396-0116-05