NDC Package 78564-001-02 Bittol Anti-bacterial Hand Gel

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:
78564-001-02
Package Description:
250 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Bittol Anti-bacterial Hand Gel
Non-Proprietary Name:
Alcohol
Substance Name:
Alcohol
Usage Information:
Provides practical cleaning without using water and soap when necessary. It used for hand cleaning. Remove all your jewerly before use. Be careful to there is no visible dirtiness on the hands and that the hands skin are not wet. It used as often as desired. Take 3-5 ml of Bittol Antibacterial Hand Gel. Rub your hands with Bittol Antibacterial Hand gel Until it is dry properly. Children under 6 years of age should be supervised when using this product.
11-Digit NDC Billing Format:
78564000102
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:
    Taha Kimya Kozmetik Ve Tuketim Urunleri Sanayi Pazarlama Limited Sirketi
    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:
    505G(a)(3)
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    08-14-2020
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    78564-001-01100 mL in 1 BOTTLE
    78564-001-03500 mL in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 78564-001-02?

    The NDC Packaged Code 78564-001-02 is assigned to a package of 250 ml in 1 bottle of Bittol Anti-bacterial Hand Gel, a human over the counter drug labeled by Taha Kimya Kozmetik Ve Tuketim Urunleri Sanayi Pazarlama Limited Sirketi. The product's dosage form is gel and is administered via topical form.

    Is NDC 78564-001 included in the NDC Directory?

    Yes, Bittol Anti-bacterial Hand Gel with product code 78564-001 is active and included in the NDC Directory. The product was first marketed by Taha Kimya Kozmetik Ve Tuketim Urunleri Sanayi Pazarlama Limited Sirketi on August 14, 2020 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 78564-001-02?

    The 11-digit format is 78564000102. 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
    5-3-278564-001-025-4-278564-0001-02