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  5. NDC Package Code: 69291-8050-2 Newgel Plus Spf

NDC Package 69291-8050-2 Newgel Plus Spf

Zinc Oxide,Sunscreen Gel Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
69291-8050-2
Package Description:
15 g in 1 BOTTLE
Product Code:
69291-8050
Proprietary Name:
Newgel Plus Spf
Non-Proprietary Name:
Zinc Oxide, Sunscreen
Substance Name:
Zinc Oxide
Usage Information:
This medication is used to treat and prevent diaper rash and other minor skin irritations (e.g., burns, cuts, scrapes). It works by forming a barrier on the skin to protect it from irritants/moisture.
11-Digit NDC Billing Format:
69291805002
NDC to RxNorm Crosswalk:
  • RxCUI: 1442087 - allantoin 0.5 % Topical Gel
  • RxCUI: 1442087 - allantoin 0.005 MG/MG Topical Gel
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Newmedical Technology, Inc.
    Dosage Form:
    Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
    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):
  • ZINC OXIDE 20 g/100g
    • Sample Package:
    No
    FDA Application Number:
    part352
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    10-01-2016
    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 69291-8050-2?

    The NDC Packaged Code 69291-8050-2 is assigned to a package of 15 g in 1 bottle of Newgel Plus Spf, a human over the counter drug labeled by Newmedical Technology, Inc.. The product's dosage form is gel and is administered via topical form.

    Is NDC 69291-8050 included in the NDC Directory?

    Yes, Newgel Plus Spf with product code 69291-8050 is active and included in the NDC Directory. The product was first marketed by Newmedical Technology, Inc. on October 01, 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 69291-8050-2?

    The 11-digit format is 69291805002. 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
    5-4-169291-8050-25-4-269291-8050-02