Ear Wax Relief Solution
NDC Package 59262-272-11

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

Package Information

Ear Wax Relief (causticum, graphite, lachesis muta venom and lycopodium clavatum spore) solution is fOR USE IN THE EAR ONLY.For adults and children, over 12 years of age:remove tamper evident seal from neck of bottletwist cap off bottletilt head sideways, squeeze plastic applicator to release 2-3 drops into ear. This formulation utilizes a solution delivery system. Marketed by Similasan Corporation, this product is identified by NDC 59262-272.

Identification & Billing

NDC Package Code
59262-272-11
Package Description
10 mL in 1 BOTTLE, DROPPER
Product Code
59262-272
11-Digit Billing Format
59262027211
Billing Unit
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
Units Per Package
10 ML

Clinical Specifications

Proprietary Name
Ear Wax Relief
Non-Proprietary Name
Causticum, Graphite, Lachesis Muta Venom And Lycopodium Clavatum Spore
Substance Name
Causticum; Graphite; Lachesis Muta Venom; Lycopodium Clavatum Spore
Dosage Form
Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Administration Route
Auricular (otic) - Administration to or by way of the ear.
Active Ingredient(s)
Usage Information
FOR USE IN THE EAR ONLY.For adults and children, over 12 years of age:remove tamper evident seal from neck of bottletwist cap off bottletilt head sideways, squeeze plastic applicator to release 2-3 drops into ear. (Tip of applicator should not enter ear canal.)keep drops in ear for several minutes by keeping head tilted or placing cotton in earuse twice daily for up to 3 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 syringechildren under 12 years of age: consult a doctor

Regulatory & Marketing

Labeler Name
Similasan Corporation
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
06-01-2003
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 59262-272-11 identifies a specific commercial package of 10 ml in 1 bottle, dropper of Ear Wax Relief, a human over the counter drug labeled by Similasan Corporation. This product is billed per "ML" milliliter and contains an estimated amount of 10 billable units per package. This solution is formulated for auricular (otic) use and contains causticum; graphite; lachesis muta venom; lycopodium clavatum spore 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 Similasan Corporation on June 01, 2003. The current certification is valid through December 31, 2026.

How is this Similasan Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 59262027211. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. There are 10 total billable units per package. 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)
59262-272-11
11-Digit CMS (5-4-2)
59262-0272-11

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