Lubricant Eye Drops
NDC Package 85185-002-10

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Lubricant Eye Drops is shake well before usingInstill 1 or 2 drops in the affected eye(s) as needed. Marketed by Solis Pharmaceuticals Inc., this product is identified by NDC 85185-002 and is authorized under FDA application M018.

Identification & Billing

NDC Package Code
85185-002-10
Package Description
1 BOTTLE, DROPPER in 1 CARTON / 10 mL in 1 BOTTLE, DROPPER
Product Code
11-Digit Billing Format
85185000210

Clinical Specifications

Proprietary Name
Lubricant Eye Drops
Dosage Form
-
Usage Information
Shake well before usingInstill 1 or 2 drops in the affected eye(s) as needed.

Regulatory & Marketing

Labeler Name
Solis Pharmaceuticals Inc.
FDA Application #
M018
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
03-01-2021
End Marketing Date
05-31-2026
Listing Expiration
05-31-2026
Exclude Flag
D
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (85185-002). Click a package code to view its specific billing and regulatory data.

2 BOTTLE, DROPPER in 1 CARTON / 10 mL in 1 BOTTLE, DROPPER

* 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 85185-002-10 identifies a specific commercial package of 1 bottle, dropper in 1 carton / 10 ml in 1 bottle, dropper of Lubricant Eye Drops, labeled by Solis Pharmaceuticals Inc.. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Solis Pharmaceuticals Inc. on March 01, 2021. The current certification is valid through May 31, 2026.

How is this Solis Pharmaceuticals Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 85185000210. 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)
85185-002-10
11-Digit CMS (5-4-2)
85185-0002-10

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