Advanced Eye Relief Eye Wash Solution/ Drops
NDC Package 24208-005-04

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

Package Information

Advanced Eye Relief Eye Wash (water solution) solution/ dropses is for use with nozzle applicator.▪flush the affected eye(s) as needed ▪control the rate of flow of solution by pressure on the bottle▪do not touch dropper tip to eye[image eye] Without Eye Cup[image eye) With Eye CupWhen using an eye cup▪rinse the cup with Bausch + Lomb Advanced Eye Relief ® eye wash immediately before each use▪avoid contamination of the rim and inside surfaces of the cup▪fill the cup half full with Bausch + Lomb Advanced Eye Relief® eye wash solution and apply the cup to the affected eye(s), pressing tightly to prevent spillage▪tilt the head backward. This formulation utilizes a solution/ drops delivery system. Marketed by Bausch & Lomb Incorporated, this product is identified by NDC 24208-005 and is authorized under FDA application M018.

Identification & Billing

NDC Package Code
24208-005-04
Package Description
1 APPLICATOR in 1 CARTON / 118 mL in 1 APPLICATOR
Product Code
24208-005
11-Digit Billing Format
24208000504
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Advanced Eye Relief Eye Wash
Non-Proprietary Name
Water Solution
Substance Name
Water
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)
WATER 99.05 mL/100mL
Usage Information
For use with nozzle applicator.▪flush the affected eye(s) as needed ▪control the rate of flow of solution by pressure on the bottle▪do not touch dropper tip to eye[image eye] Without Eye Cup[image eye) With Eye CupWhen using an eye cup▪rinse the cup with Bausch + Lomb Advanced Eye Relief ® eye wash immediately before each use▪avoid contamination of the rim and inside surfaces of the cup▪fill the cup half full with Bausch + Lomb Advanced Eye Relief® eye wash solution and apply the cup to the affected eye(s), pressing tightly to prevent spillage▪tilt the head backward. Open eyelids wide and rotate eyeball to thoroughly wash the eye▪rinse cup with clean water after each use▪replace cap after use

Regulatory & Marketing

Labeler Name
Bausch & Lomb Incorporated
Product Type
Human Otc Drug
FDA Application #
M018
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
02-02-2017
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 24208-005-04 identifies a specific commercial package of 1 applicator in 1 carton / 118 ml in 1 applicator of Advanced Eye Relief Eye Wash, a human over the counter drug labeled by Bausch & Lomb Incorporated. This solution/ drops is formulated for ophthalmic use and contains water 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 Bausch & Lomb Incorporated on February 02, 2017. The current certification is valid through December 31, 2026.

How is this Bausch & Lomb Incorporated product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 24208000504. 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)
24208-005-04
11-Digit CMS (5-4-2)
24208-0005-04

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