NDC Package 20276-980-08 Lucky Supersoft Medicated Body Triple Action

Menthol Zinc Oxide Powder 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:
20276-980-08
Package Description:
227 g in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Lucky Supersoft Medicated Body Triple Action
Non-Proprietary Name:
Menthol Zinc Oxide
Substance Name:
Menthol; Zinc Oxide
Usage Information:
■ for aduts and children 2 years and older: apply freely up to 3 or 4 times daily ■ for children under 2 years: ask a doctor ■ for best results dry skin thoroughly before applying​ Apply as needed, dry skin completely prior to using. Children under 2 years of age, consult a doctor.
11-Digit NDC Billing Format:
20276098008
NDC to RxNorm Crosswalk:
  • RxCUI: 577232 - menthol 0.15 % / zinc oxide 1 % Topical Powder
  • RxCUI: 577232 - menthol 0.0015 MG/MG / zinc oxide 0.01 MG/MG Topical Powder
  • RxCUI: 577232 - Menthol 0.0015 MG/MG / ZNO 0.01 MG/MG Topical Powder
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Delta Brands Inc
    Dosage Form:
    Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.
    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:
    part348
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    12-11-2017
    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
    20276-980-14397 g in 1 BOTTLE, PLASTIC

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 20276-980-08?

    The NDC Packaged Code 20276-980-08 is assigned to a package of 227 g in 1 bottle, plastic of Lucky Supersoft Medicated Body Triple Action, a human over the counter drug labeled by Delta Brands Inc. The product's dosage form is powder and is administered via topical form.

    Is NDC 20276-980 included in the NDC Directory?

    Yes, Lucky Supersoft Medicated Body Triple Action with product code 20276-980 is active and included in the NDC Directory. The product was first marketed by Delta Brands Inc on December 11, 2017 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 20276-980-08?

    The 11-digit format is 20276098008. 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
    5-3-220276-980-085-4-220276-0980-08