NDC Package 69842-199-64 Antibiotic

Bacitracin Zinc,Neomycin,Polymyxin B Ointment 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:
69842-199-64
Package Description:
1 TUBE in 1 CARTON / 28 g in 1 TUBE
Product Code:
Proprietary Name:
Antibiotic
Non-Proprietary Name:
Bacitracin Zinc, Neomycin, Polymyxin B
Substance Name:
Bacitracin Zinc; Neomycin Sulfate; Polymyxin B Sulfate
Usage Information:
•clean the affected area•apply a small amount of this product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times daily•may be covered with a sterile bandage
11-Digit NDC Billing Format:
69842019964
NDC to RxNorm Crosswalk:
  • RxCUI: 204602 - bacitracin 400 UNT / neomycin 3.5 MG / polymyxin B 5000 UNT per GM Topical Ointment
  • RxCUI: 204602 - bacitracin 0.4 UNT/MG / neomycin 0.0035 MG/MG / polymyxin B 5 UNT/MG Topical Ointment
  • RxCUI: 204602 - bacitracin 400 UNT / neomycin 3.5 MG (as neomycin sulfate 5 MG) / polymyxin B 5000 UNT per GM Topical Ointment
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Cvs Pharmacy
    Dosage Form:
    Ointment - A semisolid3 dosage form, usually containing <20% water and volatiles5 and >50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
    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:
    part333B
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    08-04-2016
    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
    69842-199-161 TUBE in 1 CARTON / 56 g in 1 TUBE
    69842-199-581 TUBE in 1 CARTON / 14 g in 1 TUBE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 69842-199-64?

    The NDC Packaged Code 69842-199-64 is assigned to a package of 1 tube in 1 carton / 28 g in 1 tube of Antibiotic, a human over the counter drug labeled by Cvs Pharmacy. The product's dosage form is ointment and is administered via topical form.

    Is NDC 69842-199 included in the NDC Directory?

    Yes, Antibiotic with product code 69842-199 is active and included in the NDC Directory. The product was first marketed by Cvs Pharmacy on August 04, 2016 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 69842-199-64?

    The 11-digit format is 69842019964. 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
    5-3-269842-199-645-4-269842-0199-64