NDC Package 70764-106-51 Clear Med 5%

Benzoyl Peroxide Lotion 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:
70764-106-51
Package Description:
1 TUBE in 1 BOX / 74 mL in 1 TUBE (70764-106-11)
Product Code:
Proprietary Name:
Clear Med 5%
Non-Proprietary Name:
Benzoyl Peroxide
Substance Name:
Benzoyl Peroxide
Usage Information:
This medication is used to treat mild to moderate acne. It may be used in combination with other acne treatments. When applied to the skin, benzoyl peroxide works by reducing the amount of acne-causing bacteria and by causing the skin to dry and peel. Check the ingredients on the label even if you have used the product before. The manufacturer may have changed the ingredients. Also, products with similar names may contain different ingredients meant for different purposes. Taking the wrong product could harm you.
11-Digit NDC Billing Format:
70764010651
NDC to RxNorm Crosswalk:
  • RxCUI: 106309 - benzoyl peroxide 5 % Topical Lotion
  • RxCUI: 106309 - benzoyl peroxide 50 MG/ML Topical Lotion
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Control Corrective Skincare Inc
    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):
    Sample Package:
    No
    FDA Application Number:
    M006
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    06-09-2016
    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.

    Frequently Asked Questions

    What is NDC 70764-106-51?

    The NDC Packaged Code 70764-106-51 is assigned to a package of 1 tube in 1 box / 74 ml in 1 tube (70764-106-11) of Clear Med 5%, a human over the counter drug labeled by Control Corrective Skincare Inc. The product's dosage form is lotion and is administered via topical form.

    Is NDC 70764-106 included in the NDC Directory?

    Yes, Clear Med 5% with product code 70764-106 is active and included in the NDC Directory. The product was first marketed by Control Corrective Skincare Inc on June 09, 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 70764-106-51?

    The 11-digit format is 70764010651. 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
    5-3-270764-106-515-4-270764-0106-51