NDC Package 82198-0001-1 Max Revive Plaster

Menthol,Methyl Salicylate Patch 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:
82198-0001-1
Package Description:
3 PATCH in 1 BAG / 2.3 g in 1 PATCH
Product Code:
Proprietary Name:
Max Revive Plaster
Non-Proprietary Name:
Menthol, Methyl Salicylate
Substance Name:
Menthol, Unspecified Form; Methyl Salicylate
Usage Information:
■ Adults and children 12 years of age and older: clean and dry affected area. Remove plaster from the protective layer, apply to the affected area, rub the area with your hand to secure the patch. ■ Plaster will remain effective for 8 hours. ■ Avoid using the same patch on the same area for more than 2 days. ■ Do not apply to area with excessive hair. Adhesive plaster may hurt skin upon removal. ■ Wet patch with warm water before removing from skin. ■ Children under 12 years of age: Do not use or consult a doctor.
11-Digit NDC Billing Format:
82198000101
NDC to RxNorm Crosswalk:
  • RxCUI: 1874174 - menthol 4 % / methyl salicylate 1 % Medicated Patch
  • RxCUI: 1874174 - menthol 0.04 MG/MG / methyl salicylate 0.01 MG/MG Medicated Patch
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Big 5 Nutrition Llc
    Dosage Form:
    Patch - A drug delivery system that often contains an adhesive backing that is usually applied to an external site on the body. Its ingredients either passively diffuse from, or are actively transported from, some portion of the patch. Depending upon the patch, the ingredients are either delivered to the outer surface of the body or into the body. A patch is sometimes synonymous with the terms ‘extended release film’ and ‘system’.
    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:
    505G(a)(3)
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    10-11-2021
    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 82198-0001-1?

    The NDC Packaged Code 82198-0001-1 is assigned to a package of 3 patch in 1 bag / 2.3 g in 1 patch of Max Revive Plaster, a human over the counter drug labeled by Big 5 Nutrition Llc. The product's dosage form is patch and is administered via topical form.

    Is NDC 82198-0001 included in the NDC Directory?

    Yes, Max Revive Plaster with product code 82198-0001 is active and included in the NDC Directory. The product was first marketed by Big 5 Nutrition Llc on October 11, 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 82198-0001-1?

    The 11-digit format is 82198000101. 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 5-4-1 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
    5-4-182198-0001-15-4-282198-0001-01