NDC Package 83179-001-01 Jinglinzi Ethanol Disinfectant

Ethanol Liquid 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:
83179-001-01
Package Description:
500 mL in 1 BOTTLE, SPRAY
Product Code:
Proprietary Name:
Jinglinzi Ethanol Disinfectant
Non-Proprietary Name:
Ethanol
Substance Name:
Alcohol; Hydrogen Peroxide
Usage Information:
Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.It can kill intestinal pathogenic bacteria, suppurative coccus, common bacteria of hospital infection and phthogeic yeast, and inactivate poliovirus and SARS-CoV-2
11-Digit NDC Billing Format:
83179000101
NDC to RxNorm Crosswalk:
  • RxCUI: 2384136 - ethanol 70 % / hydrogen peroxide 4 % Topical Spray
  • RxCUI: 2384136 - ethanol 0.7 ML/ML / hydrogen peroxide 40 ML/ML Topical Spray
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Shaoyang Jinglinzi Biotechnology Co., Ltd
    Dosage Form:
    Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
    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.
  • 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:
    02-14-2023
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N

    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 83179-001-01?

    The NDC Packaged Code 83179-001-01 is assigned to a package of 500 ml in 1 bottle, spray of Jinglinzi Ethanol Disinfectant, a human over the counter drug labeled by Shaoyang Jinglinzi Biotechnology Co., Ltd. The product's dosage form is liquid and is administered via topical form.

    Is NDC 83179-001 included in the NDC Directory?

    Yes, Jinglinzi Ethanol Disinfectant with product code 83179-001 is active and included in the NDC Directory. The product was first marketed by Shaoyang Jinglinzi Biotechnology Co., Ltd on February 14, 2023 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 83179-001-01?

    The 11-digit format is 83179000101. 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
    5-3-283179-001-015-4-283179-0001-01