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  5. NDC Package Code: 70512-102-30 Triple Antibiotic

NDC Package 70512-102-30 Triple Antibiotic

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
70512-102-30
Package Description:
1 TUBE in 1 CARTON / 28.4 g in 1 TUBE
Product Code:
70512-102
Proprietary Name:
Triple Antibiotic
Usage Information:
Clean the affected areaApply 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 dailyMay be covered with a sterile bandageChildren under 2 years of age - Ask the doctor
11-Digit NDC Billing Format:
70512010230
Billing Unit:
GM - Billing unit of "gram" is used when a product is measured by its weight.
NDC to RxNorm Crosswalk:
28.4 GM
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
    • Labeler Name:
    Sola Pharmaceuticals
    Sample Package:
    No
    Start Marketing Date:
    02-12-2021
    Listing Expiration Date:
    12-31-2023
    Exclude Flag:
    I
    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.

    Frequently Asked Questions

    What is NDC 70512-102-30?

    The NDC Packaged Code 70512-102-30 is assigned to a package of 1 tube in 1 carton / 28.4 g in 1 tube of Triple Antibiotic, labeled by Sola Pharmaceuticals. The product's dosage form is and is administered via form.

    Is NDC 70512-102 included in the NDC Directory?

    No, Triple Antibiotic with product code 70512-102 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Sola Pharmaceuticals on February 12, 2021 and its listing in the NDC Directory is set to expire on December 31, 2023 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 70512-102-30?

    The contents of this package are billed per "gm or gram", products billed per gram are products measured by weight. The calculated billable units for this package is 28.4.

    What is the 11-digit format for NDC 70512-102-30?

    The 11-digit format is 70512010230. 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
    5-3-270512-102-305-4-270512-0102-30