Carboxymethylcellulose Sodium, Unspecified Solution, Gel Forming / Drops
NDC Package 53014-151-05

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

Carboxymethylcellulose Sodium, Unspecified solution is a drug for further processing. This formulation utilizes a solution, gel forming / drops delivery system. Marketed by Unither Manufacturing Llc, this product is identified by NDC 53014-151.

Identification & Billing

NDC Package Code
53014-151-05
Package Description
5 VIAL, SINGLE-USE in 1 POUCH / .4 mL in 1 VIAL, SINGLE-USE
Product Code
53014-151
11-Digit Billing Format
53014015105

Clinical Specifications

Proprietary Name
Carboxymethylcellulose Sodium, Unspecified
Non-Proprietary Name
Carboxymethylcellulose Sodium, Unspecified
Substance Name
Carboxymethylcellulose Sodium, Unspecified
Dosage Form
Solution, Gel Forming / Drops - A solution, which after usually being administered in a drop-wise fashion, forms a gel.
Active Ingredient(s)
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED .5 g/100mL

Regulatory & Marketing

Labeler Name
Unither Manufacturing Llc
Product Type
Drug For Further Processing
Marketing Category
DRUG FOR FURTHER PROCESSING - A drug (other than the bulk ingredient API) that is in an interim stage of manufacture, processing, preparation, or packaging, and not ready for human or animal use.
Start Marketing Date
11-11-2013
Listing Expiration
12-31-2026
Exclude Flag
N
Unfinished Product
Yes
Sample Package
N/A

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 53014-151-05 identifies a specific commercial package of 5 vial, single-use in 1 pouch / .4 ml in 1 vial, single-use of Carboxymethylcellulose Sodium, Unspecified (UNFINISHED drug), drug for further processing labeled by Unither Manufacturing Llc. This solution, gel forming / drops is formulated for use and contains carboxymethylcellulose sodium, unspecified as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Unither Manufacturing Llc on November 11, 2013. The current certification is valid through December 31, 2026.

How is this Unither Manufacturing Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 53014015105. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
53014-151-05
11-Digit CMS (5-4-2)
53014-0151-05

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.