Eagle Liquid
NDC Package 43405-010-01

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

Package Information

Eagle (menthol methyl salicylate) liquids is ■ adults and children 12 years of age and older apply to affected area not more than 3 to 4 time daily. This formulation utilizes a liquid delivery system. Marketed by Borden Company (private) Limited, this product is identified by NDC 43405-010 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
43405-010-01
Package Description
1 BOTTLE, GLASS in 1 BOX / 85 mL in 1 BOTTLE, GLASS (43405-010-85)
Product Code
43405-010
11-Digit Billing Format
43405001001
RxNorm Crosswalk
  • RxCUI: 1654726 - menthol 14.5 % / methyl salicylate 30 % Topical Solution
  • RxCUI: 1654726 - menthol 145 MG/ML / methyl salicylate 300 MG/ML Topical Solution

Clinical Specifications

Proprietary Name
Eagle Extra Strength
Non-Proprietary Name
Menthol Methyl Salicylate
Substance Name
Menthol; Methyl Salicylate
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s)
Usage Information
■ adults and children 12 years of age and older apply to affected area not more than 3 to 4 time daily. ■ apply liberally and gently rub into affected area ■ children under 12 years of age, consult a doctor before using.

Regulatory & Marketing

Labeler Name
Borden Company (private) Limited
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
06-15-2015
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 43405-010-01 identifies a specific commercial package of 1 bottle, glass in 1 box / 85 ml in 1 bottle, glass (43405-010-85) of Eagle Extra Strength, a human over the counter drug labeled by Borden Company (private) Limited. This liquid is formulated for topical use and contains menthol; methyl salicylate 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 Borden Company (private) Limited on June 15, 2015. The current certification is valid through December 31, 2026.

How is this Borden Company (private) Limited product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 43405001001. 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)
43405-010-01
11-Digit CMS (5-4-2)
43405-0010-01

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