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  5. NDC Package Code: 70039-300-02 Professional Therapy Musclecare Pain Relieving

NDC Package 70039-300-02 Professional Therapy Musclecare Pain Relieving

Menthol,Camphor Ointment Cutaneous; 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:
70039-300-02
Package Description:
115 g in 1 TUBE
Product Code:
70039-300
Proprietary Name:
Professional Therapy Musclecare Pain Relieving
Non-Proprietary Name:
Menthol, Camphor
Substance Name:
Camphor (synthetic); Menthol
Usage Information:
This product is used as For muscle and joint pain reliefThis product is used as . Menthol 4.0%...........................Analgesic (pain relief)Camphor 4.0%........................Analgesic (pain relief)
11-Digit NDC Billing Format:
70039030002
NDC to RxNorm Crosswalk:
  • RxCUI: 900390 - camphor 4 % / menthol 4 % Topical Ointment
  • RxCUI: 900390 - camphor 0.04 MG/MG / menthol 0.04 MG/MG Topical Ointment
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Active And Innovative Inc.
    Dosage Form:
    Ointment - A semisolid3 dosage form, usually containing <20% water and volatiles5 and >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):
  • Cutaneous - Administration to the skin.
  • 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):
  • CAMPHOR (SYNTHETIC) 40 mg/g
  • MENTHOL 40 mg/g
    • 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:
    01-01-2017
    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 70039-300-02?

    The NDC Packaged Code 70039-300-02 is assigned to a package of 115 g in 1 tube of Professional Therapy Musclecare Pain Relieving, a human over the counter drug labeled by Active And Innovative Inc.. The product's dosage form is ointment and is administered via cutaneous; topical form.

    Is NDC 70039-300 included in the NDC Directory?

    Yes, Professional Therapy Musclecare Pain Relieving with product code 70039-300 is active and included in the NDC Directory. The product was first marketed by Active And Innovative Inc. on January 01, 2017 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 70039-300-02?

    The 11-digit format is 70039030002. 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
    5-3-270039-300-025-4-270039-0300-02