NDC Package 80659-301-04 Purifi Hand Sanitizer

Benzalkonium Chloride Solution 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:
80659-301-04
Package Description:
50 mL in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Purifi Hand Sanitizer
Non-Proprietary Name:
Benzalkonium Chloride
Substance Name:
Benzalkonium Chloride
Usage Information:
UsesHand sanitizing to help reduce bacteria on the skin
11-Digit NDC Billing Format:
80659030104
NDC to RxNorm Crosswalk:
  • RxCUI: 1049254 - benzalkonium chloride 0.13 % Topical Solution
  • RxCUI: 1049254 - benzalkonium chloride 1.3 MG/ML Topical Solution
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Purifi Llc
    Dosage Form:
    Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
    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:
    M007
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    12-10-2020
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    80659-301-01250 mL in 1 BOTTLE, PLASTIC
    80659-301-0260 mL in 1 BOTTLE, PLASTIC
    80659-301-033800 mL in 1 BOTTLE, PLASTIC
    80659-301-05296 mL in 1 BOTTLE, PLASTIC

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 80659-301-04?

    The NDC Packaged Code 80659-301-04 is assigned to a package of 50 ml in 1 bottle, plastic of Purifi Hand Sanitizer, a human over the counter drug labeled by Purifi Llc. The product's dosage form is solution and is administered via topical form.

    Is NDC 80659-301 included in the NDC Directory?

    Yes, Purifi Hand Sanitizer with product code 80659-301 is active and included in the NDC Directory. The product was first marketed by Purifi Llc on December 10, 2020 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 80659-301-04?

    The 11-digit format is 80659030104. 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
    5-3-280659-301-045-4-280659-0301-04