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  5. NDC Package Code: 72562-167-25 Pain Relief Liquid Roller

NDC Package 72562-167-25 Pain Relief Liquid Roller

Camphor 3.5%,Menthol 3.5% Liquid 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:
72562-167-25
Package Description:
70 g in 1 BOTTLE, PLASTIC
Product Code:
72562-167
Proprietary Name:
Pain Relief Liquid Roller
Non-Proprietary Name:
Camphor 3.5%, Menthol 3.5%
Substance Name:
Camphor (synthetic); Menthol
Usage Information:
For the temporary relief of minor aches and pain associated with simple backaches, arthritis, strains, bruises, and sprains.
11-Digit NDC Billing Format:
72562016725
NDC to RxNorm Crosswalk:
  • RxCUI: 2467741 - camphor 3.5 % / menthol 3.5 % Topical Solution
  • RxCUI: 2467741 - camphor 35 MG/ML / menthol 35 MG/ML Topical Solution
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Tommie Copper, Inc.
    Dosage Form:
    Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
    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.
    • Active Ingredient(s):
  • CAMPHOR (SYNTHETIC) 3.5 g/100g
  • MENTHOL 3.5 g/100g
    • 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:
    08-19-2021
    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 72562-167-25?

    The NDC Packaged Code 72562-167-25 is assigned to a package of 70 g in 1 bottle, plastic of Pain Relief Liquid Roller, a human over the counter drug labeled by Tommie Copper, Inc.. The product's dosage form is liquid and is administered via topical form.

    Is NDC 72562-167 included in the NDC Directory?

    Yes, Pain Relief Liquid Roller with product code 72562-167 is active and included in the NDC Directory. The product was first marketed by Tommie Copper, Inc. on August 19, 2021 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 72562-167-25?

    The 11-digit format is 72562016725. 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
    5-3-272562-167-255-4-272562-0167-25