Target Lubricant Eye Drops High Performance Solution/ Drops
NDC Package 11673-101-01

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

Package Information

Target Lubricant Eye Drops High Performance (polyethylene glycol 400, propylene glycol) solution/ dropses is uses• for the temporary relief of burning and irritation due to dryness of the eye. This formulation utilizes a solution/ drops delivery system. Marketed by Target Corporation, this product is identified by NDC 11673-101 and is authorized under FDA application M018.

Identification & Billing

NDC Package Code
11673-101-01
Package Description
1 BOTTLE, DROPPER in 1 BOX / 15 mL in 1 BOTTLE, DROPPER
Product Code
11673-101
11-Digit Billing Format
11673010101
RxNorm Crosswalk
  • RxCUI: 477589 - polyethylene glycol 400, 0.4 % / propylene glycol 0.3 % Ophthalmic Solution
  • RxCUI: 477589 - polyethylene glycol 400 4 MG/ML / propylene glycol 3 MG/ML Ophthalmic Solution
  • RxCUI: 477589 - PEG 400 0.4 % / propylene glycol 0.3 % Ophthalmic Solution

Clinical Specifications

Proprietary Name
Target Lubricant Eye Drops High Performance
Non-Proprietary Name
Polyethylene Glycol 400, Propylene Glycol
Substance Name
Polyethylene Glycol 400; Propylene Glycol
Dosage Form
Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
Administration Route
Ophthalmic - Administration to the external eye.
Active Ingredient(s)
Usage Information
Uses• for the temporary relief of burning and irritation due to dryness of the eye

Regulatory & Marketing

Labeler Name
Target Corporation
Product Type
Human Otc Drug
FDA Application #
M018
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
02-11-2019
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

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 11673-101-01 identifies a specific commercial package of 1 bottle, dropper in 1 box / 15 ml in 1 bottle, dropper of Target Lubricant Eye Drops High Performance, a human over the counter drug labeled by Target Corporation. This solution/ drops is formulated for ophthalmic use and contains polyethylene glycol 400; propylene glycol 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 Target Corporation on February 11, 2019. The current certification is valid through December 31, 2026.

How is this Target Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 11673010101. 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)
11673-101-01
11-Digit CMS (5-4-2)
11673-0101-01

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