Maximum Strength Blue Emu Pain Relief Spray
NDC Package 69993-100-04

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

Package Information

Maximum Strength Blue Emu Pain Relief (trolamine salicylate) sprays is usesTemporarily relieves pain associated with:  arthritis, simple backache, muscle strains, sprains, bruises, and cramps. This formulation utilizes a spray delivery system. Marketed by Kingsway Pharmaceuticals Dba Nfi, Llc, this product is identified by NDC 69993-100 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
69993-100-04
Package Description
118 mL in 1 CAN
Product Code
69993-100
11-Digit Billing Format
69993010004
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Maximum Strength Blue Emu Pain Relief Blu Emu
Non-Proprietary Name
Trolamine Salicylate
Substance Name
Trolamine Salicylate
Dosage Form
Spray - A liquid minutely divided as by a jet of air or steam.
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)
TROLAMINE SALICYLATE 10 g/100mL
Usage Information
UsesTemporarily relieves pain associated with:  arthritis, simple backache, muscle strains, sprains, bruises, and cramps.

Regulatory & Marketing

Labeler Name
Kingsway Pharmaceuticals Dba Nfi, Llc
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
06-04-2012
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 69993-100-04 identifies a specific commercial package of 118 ml in 1 can of Maximum Strength Blue Emu Pain Relief Blu Emu, a human over the counter drug labeled by Kingsway Pharmaceuticals Dba Nfi, Llc. This spray is formulated for topical use and contains trolamine 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 Kingsway Pharmaceuticals Dba Nfi, Llc on June 04, 2012. The current certification is valid through December 31, 2026.

How is this Kingsway Pharmaceuticals Dba Nfi, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 69993010004. 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)
69993-100-04
11-Digit CMS (5-4-2)
69993-0100-04

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