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  5. NDC Package Code: 69993-100-04 Maximum Strength Blue Emu Pain Relief Blu Emu

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

Trolamine Salicylate Spray Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
69993-100-04
Package Description:
118 mL in 1 CAN
Product Code:
69993-100
Proprietary Name:
Maximum Strength Blue Emu Pain Relief Blu Emu
Non-Proprietary Name:
Trolamine Salicylate
Substance Name:
Trolamine Salicylate
Usage Information:
UsesTemporarily relieves pain associated with:  arthritis, simple backache, muscle strains, sprains, bruises, and cramps.
11-Digit NDC Billing Format:
69993010004
NDC to RxNorm Crosswalk:
  • RxCUI: 1048119 - trolamine salicylate 10 % Topical Spray
  • RxCUI: 1048119 - trolamine salicylate 100 MG/ML Topical Spray
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Nfi, Llc
    Dosage Form:
    Spray - A liquid minutely divided as by a jet of air or steam.
    Administration Route(s):
  • 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
    • Sample Package:
    No
    FDA Application Number:
    part348
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    06-04-2012
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    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 disclaimer below.

    Frequently Asked Questions

    What is NDC 69993-100-04?

    The NDC Packaged Code 69993-100-04 is assigned to a package of 118 ml in 1 can of Maximum Strength Blue Emu Pain Relief Blu Emu, a human over the counter drug labeled by Nfi, Llc. The product's dosage form is spray and is administered via topical form.

    Is NDC 69993-100 included in the NDC Directory?

    Yes, Maximum Strength Blue Emu Pain Relief Blu Emu with product code 69993-100 is active and included in the NDC Directory. The product was first marketed by Nfi, Llc on June 04, 2012 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 69993-100-04?

    The 11-digit format is 69993010004. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-269993-100-045-4-269993-0100-04