Ear Wax Removal System
NDC Package 49035-554-07

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Ear Wax Removal System is tilt head sideways and place 5 to 10 drops into eartip of applicator should not enter ear canalkeep drops in ear for several minutes by keeping head tilted or placing cotton in the earuse twice daily for up to 4 days if needed, or as directed by a doctorany wax remaining after treatment may be removed by gently flushing the ear with warm water, using a soft rubber bulb ear syringe​Children under 12 years of age: consult a doctor. Marketed by Walmart, this product is identified by NDC 49035-554 and is authorized under FDA application part344.

Identification & Billing

NDC Package Code
49035-554-07
Package Description
1 KIT in 1 KIT * 15 mL in 1 BOTTLE (49035-552-01)
Product Code
49035-554
11-Digit Billing Format
49035055407
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Ear Wax Removal System
Dosage Form
-
Usage Information
Tilt head sideways and place 5 to 10 drops into eartip of applicator should not enter ear canalkeep drops in ear for several minutes by keeping head tilted or placing cotton in the earuse twice daily for up to 4 days if needed, or as directed by a doctorany wax remaining after treatment may be removed by gently flushing the ear with warm water, using a soft rubber bulb ear syringe​Children under 12 years of age: consult a doctor.

Regulatory & Marketing

Labeler Name
Walmart
FDA Application #
part344
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
10-04-2011
Listing Expiration
12-31-2019
Exclude Flag
I
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 49035-554-07 identifies a specific commercial package of 1 kit in 1 kit * 15 ml in 1 bottle (49035-552-01) of Ear Wax Removal System, labeled by Walmart. 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 Walmart on October 04, 2011. The current certification is valid through December 31, 2019.

How is this Walmart product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 49035055407. 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)
49035-554-07
11-Digit CMS (5-4-2)
49035-0554-07

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