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  5. NDC Package Code: 10157-2101-1 Blistex Stridex Spot And T-zone Acne Cleargel

NDC Package 10157-2101-1 Blistex Stridex Spot And T-zone Acne Cleargel

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:
10157-2101-1
Package Description:
1 JAR in 1 CARTON / 28.35 g in 1 JAR
Product Code:
10157-2101
Proprietary Name:
Blistex Stridex Spot And T-zone Acne Cleargel
Usage Information:
Clean the skin thoroughly before applying this productcover the entire affected area with a thin layer one to three times dailybecause excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctorif bothersome dryness or peeling occurs, reduce application to once a day or every other daykeep away from eyes, lips and other mucous membranes
11-Digit NDC Billing Format:
10157210101
NDC to RxNorm Crosswalk:
  • RxCUI: 1730425 - Stridex Spot and T-Zone 2 % Topical Gel
  • RxCUI: 1730425 - salicylic acid 0.02 MG/MG Topical Gel [Stridex]
  • RxCUI: 1730425 - Stridex 0.02 MG/MG Topical Gel
  • RxCUI: 346298 - salicylic acid 2 % Topical Gel
  • RxCUI: 346298 - salicylic acid 0.02 MG/MG Topical Gel
    • Labeler Name:
    Blistex Inc
    Sample Package:
    No
    Start Marketing Date:
    01-04-2016
    Listing Expiration Date:
    12-31-2019
    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 10157-2101-1?

    The NDC Packaged Code 10157-2101-1 is assigned to a package of 1 jar in 1 carton / 28.35 g in 1 jar of Blistex Stridex Spot And T-zone Acne Cleargel, labeled by Blistex Inc. The product's dosage form is and is administered via form.

    Is NDC 10157-2101 included in the NDC Directory?

    No, Blistex Stridex Spot And T-zone Acne Cleargel with product code 10157-2101 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Blistex Inc on January 04, 2016 and its listing in the NDC Directory is set to expire on December 31, 2019 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 10157-2101-1?

    The 11-digit format is 10157210101. 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 5-4-1 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
    5-4-110157-2101-15-4-210157-2101-01