NDC Package 66513-220-14 Bronco Rub

Camphor Eucalyptus Menthol Ointment 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:
66513-220-14
Package Description:
39 g in 1 JAR
Product Code:
Proprietary Name:
Bronco Rub
Non-Proprietary Name:
Camphor Eucalyptus Menthol
Substance Name:
Camphor (synthetic); Eucalyptus Oil; Menthol
Usage Information:
See important warnings under "When using this product" section•adults and children 2 years and over rub a thick layer on chest and throat or rub on sore aching muscles •cover with a warm, dry cloth if desired • keep clothing loose about throat/chest to help vapors reach the nose/mouth • repeat up to three times per 24 hours or as directed by doctor • children under 2 years: do not use 
11-Digit NDC Billing Format:
66513022014
NDC to RxNorm Crosswalk:
  • RxCUI: 727137 - camphor 4.8 % / eucalyptus oil 1.2 % / menthol 2.6 % Topical Ointment
  • RxCUI: 727137 - camphor 0.048 MG/MG / Eucalyptus oil 0.012 MG/MG / menthol 0.026 MG/MG Topical Ointment
  • RxCUI: 727137 - camphor 4.8 % / eucalyptus oil 1.2 % / menthol 2.6 % Chest Rub
  • RxCUI: 727137 - camphor 4.8 % / eucalyptus oil 1.2 % / menthol 2.6 % Topical Stick
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Distribuidora De Alimentos Naturales Y Nutricionales, S.a. De C.v
    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):
  • 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:
    M012
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    08-15-2014
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N

    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 66513-220-14?

    The NDC Packaged Code 66513-220-14 is assigned to a package of 39 g in 1 jar of Bronco Rub, a human over the counter drug labeled by Distribuidora De Alimentos Naturales Y Nutricionales, S.a. De C.v. The product's dosage form is ointment and is administered via topical form.

    Is NDC 66513-220 included in the NDC Directory?

    Yes, Bronco Rub with product code 66513-220 is active and included in the NDC Directory. The product was first marketed by Distribuidora De Alimentos Naturales Y Nutricionales, S.a. De C.v on August 15, 2014 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 66513-220-14?

    The 11-digit format is 66513022014. 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
    5-3-266513-220-145-4-266513-0220-14