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  5. NDC Package Code: 53329-202-85 Hand Sanitizer

NDC Package 53329-202-85 Hand Sanitizer

Ethyl Alcohol Gel Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
53329-202-85
Package Description:
354 mL in 1 BOTTLE
Product Code:
53329-202
Proprietary Name:
Hand Sanitizer
Non-Proprietary Name:
Ethyl Alcohol
Substance Name:
Alcohol
Usage Information:
Wet hands thoroughly with product and allow to dry without wiping For children under 6, use only under adult supervision Not recommended for infants.
11-Digit NDC Billing Format:
53329020285
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:
    Medline Industries, Lp
    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 70 mL/100mL
    • Sample Package:
    No
    FDA Application Number:
    part333E
    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:
    04-06-2015
    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
    53329-202-04118 mL in 1 BOTTLE
    53329-202-08236 mL in 1 BOTTLE
    53329-202-1359 mL in 1 BOTTLE
    53329-202-741200 mL in 1 BOTTLE
    53329-202-841000 mL in 1 BAG

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 53329-202-85?

    The NDC Packaged Code 53329-202-85 is assigned to a package of 354 ml in 1 bottle of Hand Sanitizer, a human over the counter drug labeled by Medline Industries, Lp. The product's dosage form is gel and is administered via topical form.

    Is NDC 53329-202 included in the NDC Directory?

    Yes, Hand Sanitizer with product code 53329-202 is active and included in the NDC Directory. The product was first marketed by Medline Industries, Lp on April 06, 2015 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 53329-202-85?

    The 11-digit format is 53329020285. 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
    5-3-253329-202-855-4-253329-0202-85