NDC Package 79032-202-51 Hand Sanitizer

View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
79032-202-51
Package Description:
4 BOTTLE, PLASTIC in 1 BOX / 5 L in 1 BOTTLE, PLASTIC (79032-202-50)
Product Code:
Proprietary Name:
Hand Sanitizer
Usage Information:
This product is used as Hydro-Alcoholic gel for hands decontamination, containing a hand-protecting agent. Its gel-texture allows a fast, practical, and effective use if the product disinfecting solution no foaming, without rinsing, nor wiping, without residues, eliminates the odors of bacterial proliferation. Hydro-Alcoholic gel for hands decontamination, containing a hand-protecting agent. Its gel-texture allows a fast, practical, and effective use if the product disinfecting solution no foaming, without rinsing, nor wiping, without residues, eliminates the odors of bacterial proliferation. The Hand sanitizing wipe cleans, disinfects, deodorizes, allows the destruction of microbes, germs, bacteria, and facilitates their total elimination. Hand sanitizing is a bactericidal, fungicidal, virucidal wipe for an effective disinection. Hand sanitizing - by its composition - ensures you a total protection of your hands with components such as glycerin and arnica
11-Digit NDC Billing Format:
79032020251
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
  • Labeler Name:
    Actalys
    Sample Package:
    No
    Start Marketing Date:
    07-15-2020
    Listing Expiration Date:
    12-31-2021
    Exclude Flag:
    I
    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 79032-202-51?

    The NDC Packaged Code 79032-202-51 is assigned to a package of 4 bottle, plastic in 1 box / 5 l in 1 bottle, plastic (79032-202-50) of Hand Sanitizer, labeled by Actalys. The product's dosage form is and is administered via form.

    Is NDC 79032-202 included in the NDC Directory?

    No, Hand Sanitizer with product code 79032-202 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Actalys on July 15, 2020 and its listing in the NDC Directory is set to expire on December 31, 2021 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 79032-202-51?

    The 11-digit format is 79032020251. 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
    5-3-279032-202-515-4-279032-0202-51