NDC Package 55715-001-12 Zepol Topical Analgesic

Camphor,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:
55715-001-12
Package Description:
12 CAN in 1 BOX / 10 g in 1 CAN
Product Code:
Proprietary Name:
Zepol Topical Analgesic
Non-Proprietary Name:
Camphor, Menthol
Substance Name:
Camphor (synthetic); Menthol
Usage Information:
-Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4  times daily. -Children under 2 years of age: Consult a physician.
11-Digit NDC Billing Format:
55715000112
NDC to RxNorm Crosswalk:
  • RxCUI: 1044238 - camphor 6.55 % / menthol 6.55 % Topical Ointment
  • RxCUI: 1044238 - camphor 0.07 MG/MG / menthol 0.07 MG/MG Topical Ointment
  • RxCUI: 1044238 - camphor 0.065 MG/MG / menthol 0.065 MG/MG Topical Ointment
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Laboratorios Zepol S.a.
    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:
    M017
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    10-05-2009
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    55715-001-0130 g in 1 TUBE
    55715-001-901 TUBE in 1 BOX / 90 g in 1 TUBE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 55715-001-12?

    The NDC Packaged Code 55715-001-12 is assigned to a package of 12 can in 1 box / 10 g in 1 can of Zepol Topical Analgesic, a human over the counter drug labeled by Laboratorios Zepol S.a.. The product's dosage form is ointment and is administered via topical form.

    Is NDC 55715-001 included in the NDC Directory?

    Yes, Zepol Topical Analgesic with product code 55715-001 is active and included in the NDC Directory. The product was first marketed by Laboratorios Zepol S.a. on October 05, 2009 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 55715-001-12?

    The 11-digit format is 55715000112. 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
    5-3-255715-001-125-4-255715-0001-12