NDC Package 59118-837-01 Osteo Bi-flex Joint Health Pain Relieving

Menthol,Methyl Salicylate Cream Topical - View Billable Units, 11-Digit Format, RxNorm

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:
59118-837-01
Package Description:
1 TUBE in 1 BOX / 71 g in 1 TUBE
Product Code:
Proprietary Name:
Osteo Bi-flex Joint Health Pain Relieving
Non-Proprietary Name:
Menthol, Methyl Salicylate
Substance Name:
Menthol; Methyl Salicylate
Usage Information:
Adults and children 12 years of age and older: Apply to affected area not more than 3 to 4 times daily. For best results apply daily or as directed by a physicianAfter applying, wash hands with soap and water. Children under 12 years of age: consult a doctor.
11-Digit NDC Billing Format:
59118083701
NDC to RxNorm Crosswalk:
  • RxCUI: 1940367 - menthol 5 % / methyl salicylate 10 % Topical Cream
  • RxCUI: 1940367 - menthol 50 MG/ML / methyl salicylate 100 MG/ML Topical Cream
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Rexall Sundown, 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.
  • Sample Package:
    No
    FDA Application Number:
    M017
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    08-01-2017
    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 59118-837-01?

    The NDC Packaged Code 59118-837-01 is assigned to a package of 1 tube in 1 box / 71 g in 1 tube of Osteo Bi-flex Joint Health Pain Relieving, a human over the counter drug labeled by Rexall Sundown, Llc. The product's dosage form is cream and is administered via topical form.

    Is NDC 59118-837 included in the NDC Directory?

    Yes, Osteo Bi-flex Joint Health Pain Relieving with product code 59118-837 is active and included in the NDC Directory. The product was first marketed by Rexall Sundown, Llc on August 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 59118-837-01?

    The 11-digit format is 59118083701. 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
    5-3-259118-837-015-4-259118-0837-01