NDC Package 59088-488-07 Camphotrol

Camphor,Menthol Gel 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:
59088-488-07
Package Description:
85 g in 1 BOTTLE, WITH APPLICATOR
Product Code:
Proprietary Name:
Camphotrol
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 ■ use only as directed
11-Digit NDC Billing Format:
59088048807
Billing Unit:
GM - Billing unit of "gram" is used when a product is measured by its weight.
NDC to RxNorm Crosswalk:
85 GM
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:
    Puretek Corporation
    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):
  • 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:
    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:
    01-18-2022
    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 59088-488-07?

    The NDC Packaged Code 59088-488-07 is assigned to a package of 85 g in 1 bottle, with applicator of Camphotrol, a human over the counter drug labeled by Puretek Corporation. The product's dosage form is gel and is administered via topical form.This product is billed per "GM" gram and contains an estimated amount of 85 billable units per package.

    Is NDC 59088-488 included in the NDC Directory?

    Yes, Camphotrol with product code 59088-488 is active and included in the NDC Directory. The product was first marketed by Puretek Corporation on January 18, 2022 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 NDC billing unit for package 59088-488-07?

    The contents of this package are billed per "gm or gram", products billed per gram are products measured by weight. The calculated billable units for this package is 85.

    What is the 11-digit format for NDC 59088-488-07?

    The 11-digit format is 59088048807. 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
    5-3-259088-488-075-4-259088-0488-07