Vedlube Ointment
NDC Package 50989-476-98

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

Package Information

Vedlube (mineral oil and white petrolatum lubricant eye ointment) ointment is pull down lower lid of the affected eye and apply a small amount (one-fourth inch) of ointment to the inside of the eyeid every 3-4 hours or as directed by a doctor. This formulation utilizes a ointment delivery system. Marketed by Vedco Inc, this product is identified by NDC 50989-476 and is authorized under FDA application M018.

Identification & Billing

NDC Package Code
50989-476-98
Package Description
1 TUBE in 1 CARTON / 3.5 g in 1 TUBE
Product Code
50989-476
11-Digit Billing Format
50989047698

Clinical Specifications

Proprietary Name
Vedlube
Non-Proprietary Name
Mineral Oil And White Petrolatum Lubricant Eye Ointment
Substance Name
Mineral Oil; White Petrolatum
Dosage Form
Ointment - A semisolid3 dosage form, usually containing <20% water and volatiles5 and >50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
Administration Route
Ophthalmic - Administration to the external eye.
Active Ingredient(s)
Usage Information
Pull down lower lid of the affected eye and apply a small amount (one-fourth inch) of ointment to the inside of the eyeid every 3-4 hours or as directed by a doctor.

Regulatory & Marketing

Labeler Name
Vedco Inc
Product Type
Human Otc Drug
FDA Application #
M018
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
07-31-2026
Listing Expiration
12-31-2027
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 50989-476-98 identifies a specific commercial package of 1 tube in 1 carton / 3.5 g in 1 tube of Vedlube, a human over the counter drug labeled by Vedco Inc. This ointment is formulated for ophthalmic use and contains mineral oil; white petrolatum 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 Vedco Inc on July 31, 2026. The current certification is valid through December 31, 2027.

How is this Vedco Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 50989047698. 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)
50989-476-98
11-Digit CMS (5-4-2)
50989-0476-98

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