1. Home
  2. Labeler Index
  3. Skaffles Group
  4. 77720-033
  5. NDC Package Code: 77720-033-01 Moxie Hand Sanitizing Gel

NDC Package 77720-033-01 Moxie Hand Sanitizing Gel

Alcohol Gel 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:
77720-033-01
Package Description:
500 mL in 1 PACKAGE
Product Code:
77720-033
Proprietary Name:
Moxie Hand Sanitizing Gel
Non-Proprietary Name:
Alcohol
Substance Name:
Alcohol
Usage Information:
Pump a small amount in your palm and briskly rub hands together until dry.Children under 6 years of age should be supervised when in use.
11-Digit NDC Billing Format:
77720003301
NDC to RxNorm Crosswalk:
  • RxCUI: 2282911 - ethanol 71 % Topical Gel
  • RxCUI: 2282911 - ethanol 0.71 ML/ML Topical Gel
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Skaffles Group
    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):
  • ALCOHOL 71 mL/100mL
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date:
    05-15-2024
    Listing Expiration Date:
    12-31-2025
    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 77720-033-01?

    The NDC Packaged Code 77720-033-01 is assigned to a package of 500 ml in 1 package of Moxie Hand Sanitizing Gel, a human over the counter drug labeled by Skaffles Group. The product's dosage form is gel and is administered via topical form.

    Is NDC 77720-033 included in the NDC Directory?

    Yes, Moxie Hand Sanitizing Gel with product code 77720-033 is active and included in the NDC Directory. The product was first marketed by Skaffles Group on May 15, 2024 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 77720-033-01?

    The 11-digit format is 77720003301. 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
    5-3-277720-033-015-4-277720-0033-01