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  5. NDC Package Code: 69396-110-30 Muscle Rub Cream

NDC Package 69396-110-30 Muscle Rub Cream

Menthol 10%,Methyl Salicylate 15% Cream 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:
69396-110-30
Package Description:
1 TUBE in 1 BOX / 85 g in 1 TUBE
Product Code:
69396-110
Proprietary Name:
Muscle Rub Cream
Non-Proprietary Name:
Menthol 10%, Methyl Salicylate 15%
Substance Name:
Menthol; Methyl Salicylate
Usage Information:
For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises and sprains
11-Digit NDC Billing Format:
69396011030
NDC to RxNorm Crosswalk:
  • RxCUI: 311498 - menthol 10 % / methyl salicylate 15 % Topical Cream
  • RxCUI: 311498 - menthol 100 MG/ML / methyl salicylate 150 MG/ML Topical Cream
  • RxCUI: 311498 - menthol 10 GM / methyl salicylate 15 GM per 100 GM Topical Cream
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Trifecta Pharmaceuticals Usa, Llc.
    Dosage Form:
    Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
    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):
  • MENTHOL 10 g/100g
  • METHYL SALICYLATE 15 g/100g
    • Sample Package:
    No
    FDA Application Number:
    M017
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    06-04-2022
    Listing Expiration Date:
    12-31-2025
    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 69396-110-30?

    The NDC Packaged Code 69396-110-30 is assigned to a package of 1 tube in 1 box / 85 g in 1 tube of Muscle Rub Cream, a human over the counter drug labeled by Trifecta Pharmaceuticals Usa, Llc.. The product's dosage form is cream and is administered via topical form.

    Is NDC 69396-110 included in the NDC Directory?

    Yes, Muscle Rub Cream with product code 69396-110 is active and included in the NDC Directory. The product was first marketed by Trifecta Pharmaceuticals Usa, Llc. on June 04, 2022 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 69396-110-30?

    The 11-digit format is 69396011030. 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
    5-3-269396-110-305-4-269396-0110-30