NDC Package 80711-002-02 Hand Sanitizer

Alcohol 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:
80711-002-02
Package Description:
5000 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Hand Sanitizer
Non-Proprietary Name:
Alcohol
Substance Name:
Alcohol
Usage Information:
Place enough product on hands to cover all surfaces. Rub hands together until dry.Supervise children under 6 years of age when using this product to avoid swallowing.
11-Digit NDC Billing Format:
80711000202
NDC to RxNorm Crosswalk:
  • RxCUI: 581662 - ethanol 70 % Topical Gel
  • RxCUI: 581662 - ethanol 0.7 ML/ML Topical Gel
  • RxCUI: 581662 - ethyl alcohol 70 % Topical Gel
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Ivm Especialidades Quimicas, S.a. De C.v.
    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:
    part333A
    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:
    05-07-2021
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    80711-002-011000 mL in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 80711-002-02?

    The NDC Packaged Code 80711-002-02 is assigned to a package of 5000 ml in 1 bottle of Hand Sanitizer, a human over the counter drug labeled by Ivm Especialidades Quimicas, S.a. De C.v.. The product's dosage form is gel and is administered via topical form.

    Is NDC 80711-002 included in the NDC Directory?

    Yes, Hand Sanitizer with product code 80711-002 is active and included in the NDC Directory. The product was first marketed by Ivm Especialidades Quimicas, S.a. De C.v. on May 07, 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 80711-002-02?

    The 11-digit format is 80711000202. 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
    5-3-280711-002-025-4-280711-0002-02