Soothe Solution/ Drops
NDC Package 24208-495-28

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

Package Information

Soothe (glycerin and propylene glycol) solution/ dropses is •to open, completely twist off tab•instill 1 to 2 drops in the affected eye(s) as needed. This formulation utilizes a solution/ drops delivery system. Marketed by Bausch & Lomb Incorporated, this product is identified by NDC 24208-495 and is authorized under FDA application M018.

Identification & Billing

NDC Package Code
24208-495-28
Package Description
28 VIAL, SINGLE-USE in 1 CARTON / .6 mL in 1 VIAL, SINGLE-USE
Product Code
11-Digit Billing Format
24208049528
RxNorm Crosswalk
  • RxCUI: 1098601 - Soothe Lubricant 0.6 % / 0.6 % Ophthalmic Solution
  • RxCUI: 1098601 - glycerin 6 MG/ML / propylene glycol 6 MG/ML Ophthalmic Solution [Soothe Lubricant Eye Drops]
  • RxCUI: 1098601 - Soothe Lubricant Eye Drops (glycerin 0.6 % / propylene glycol 0.6 % ) Ophthalmic Solution
  • RxCUI: 832115 - glycerin 0.6 % / propylene glycol 0.6 % Ophthalmic Solution
  • RxCUI: 832115 - glycerin 6 MG/ML / propylene glycol 6 MG/ML Ophthalmic Solution

Clinical Specifications

Proprietary Name
Soothe
Non-Proprietary Name
Glycerin And Propylene Glycol
Substance Name
Glycerin; 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.
Usage Information
•to open, completely twist off tab•instill 1 to 2 drops in the affected eye(s) as needed

Regulatory & Marketing

Labeler Name
Bausch & Lomb Incorporated
Product Type
Human Otc Drug
FDA Application #
M018
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
08-26-2010
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (24208-495). Click a package code to view its specific billing and regulatory data.

30 VIAL, SINGLE-USE in 1 CARTON / .6 mL in 1 VIAL, SINGLE-USE

* 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 24208-495-28 identifies a specific commercial package of 28 vial, single-use in 1 carton / .6 ml in 1 vial, single-use of Soothe, a human over the counter drug labeled by Bausch & Lomb Incorporated. This solution/ drops is formulated for ophthalmic use and contains glycerin; 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 Bausch & Lomb Incorporated on August 26, 2010. 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: 24208049528. 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)
24208-495-28
11-Digit CMS (5-4-2)
24208-0495-28

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