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  5. NDC Package Code: 70039-283-07 Professional Therapy Musclecare Pain Relieving Gel Extra Strength

NDC Package 70039-283-07 Professional Therapy Musclecare Pain Relieving Gel Extra Strength

Camphor,Menthol Gel 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:
70039-283-07
Package Description:
1 g in 1 BOTTLE, WITH APPLICATOR
Product Code:
70039-283
Proprietary Name:
Professional Therapy Musclecare Pain Relieving Gel Extra Strength
Non-Proprietary Name:
Camphor, Menthol
Substance Name:
Camphor (synthetic); Menthol
Usage Information:
Adults and children 12 years of age or older: Using the roll-on applicator massage a liberal amount of gel directly on the affected area not more than 3 to 4 times daily. Children under the age of 12: Do not use, consult a doctor.
11-Digit NDC Billing Format:
70039028307
NDC to RxNorm Crosswalk:
  • RxCUI: 1039731 - camphor 4 % / menthol 10 % Topical Gel
  • RxCUI: 1039731 - camphor 0.04 MG/MG / menthol 0.1 MG/MG Topical Gel
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Active And Innovative Inc.
    Dosage Form:
    Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
    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 100 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:
    06-01-2015
    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 70039-283-07?

    The NDC Packaged Code 70039-283-07 is assigned to a package of 1 g in 1 bottle, with applicator of Professional Therapy Musclecare Pain Relieving Gel Extra Strength, a human over the counter drug labeled by Active And Innovative Inc.. The product's dosage form is gel and is administered via cutaneous; topical form.

    Is NDC 70039-283 included in the NDC Directory?

    Yes, Professional Therapy Musclecare Pain Relieving Gel Extra Strength with product code 70039-283 is active and included in the NDC Directory. The product was first marketed by Active And Innovative Inc. on June 01, 2015 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 70039-283-07?

    The 11-digit format is 70039028307. 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
    5-3-270039-283-075-4-270039-0283-07