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  5. NDC Package Code: 59998-101-12 Biocence

NDC Package 59998-101-12 Biocence

Eucalyptol Thymol Lotion 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:
59998-101-12
Package Description:
60 mL in 1 BOTTLE
Product Code:
59998-101
Proprietary Name:
Biocence
Non-Proprietary Name:
Eucalyptol Thymol
Substance Name:
Eucalyptol; Thymol
Usage Information:
USESA MULTIPLE USE ANTISEPTICCONTAINING PREPARATION DESIGNED FOR FREQUENT USE WITHOUT WATER AS AN ANTISEPTIC HANDWASH AND FIRST AID ANTISEPTIC.HELPS TO PROTECT AGAINST SKIN INFECTION AND TO HELP PREVENT CROSS CONTAMINATION IN CUTS, SCRAPES, BURNS, AND OR SECONDARY INFECTIONS.
11-Digit NDC Billing Format:
59998010112
NDC to RxNorm Crosswalk:
  • RxCUI: 1356343 - eucalyptol 0.091 % / thymol 0.063 % Topical Lotion
  • RxCUI: 1356343 - eucalyptol 0.91 MG/ML / thymol 0.63 MG/ML Topical Lotion
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Bio-germ Protection Llc
    Dosage Form:
    Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2
    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):
  • EUCALYPTOL .091 g/100mL
  • THYMOL .063 g/100mL
    • Sample Package:
    No
    FDA Application Number:
    M003
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    10-26-2012
    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
    59998-101-1012 mL in 1 APPLICATOR
    59998-101-14118 mL in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 59998-101-12?

    The NDC Packaged Code 59998-101-12 is assigned to a package of 60 ml in 1 bottle of Biocence, a human over the counter drug labeled by Bio-germ Protection Llc. The product's dosage form is lotion and is administered via topical form.

    Is NDC 59998-101 included in the NDC Directory?

    Yes, Biocence with product code 59998-101 is active and included in the NDC Directory. The product was first marketed by Bio-germ Protection Llc on October 26, 2012 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 59998-101-12?

    The 11-digit format is 59998010112. 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
    5-3-259998-101-125-4-259998-0101-12