NDC Package 72197-001-08 Pharmacys Prescription Analgesic Gel

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:
72197-001-08
Package Description:
227 g in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Pharmacys Prescription Analgesic Gel
Non-Proprietary Name:
Menthol
Substance Name:
Menthol
Usage Information:
Uses: For the temporary relief of minor aches and pains of muscles and joints associated with - simple backache - arthritis - strains - bruses - sprains When using this product- avoid contact with eyes- do not bandage tightly- do not apply to wounds or damaged skin- do not use with heating pads or other heating devices
11-Digit NDC Billing Format:
72197000108
NDC to RxNorm Crosswalk:
  • RxCUI: 1039043 - menthol 1 % Topical Gel
  • RxCUI: 1039043 - menthol 0.01 MG/MG Topical Gel
  • Product Type:
    Human Otc Drug
    Labeler Name:
    American Consumer Products Corp
    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.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    part346
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    08-31-2018
    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 72197-001-08?

    The NDC Packaged Code 72197-001-08 is assigned to a package of 227 g in 1 bottle, plastic of Pharmacys Prescription Analgesic Gel, a human over the counter drug labeled by American Consumer Products Corp. The product's dosage form is gel and is administered via topical form.

    Is NDC 72197-001 included in the NDC Directory?

    Yes, Pharmacys Prescription Analgesic Gel with product code 72197-001 is active and included in the NDC Directory. The product was first marketed by American Consumer Products Corp on August 31, 2018 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 72197-001-08?

    The 11-digit format is 72197000108. 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
    5-3-272197-001-085-4-272197-0001-08