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  5. NDC Package Code: 68605-2002-2 End-zit

NDC Package 68605-2002-2 End-zit

Sulfur Lotion, Augmented 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:
68605-2002-2
Package Description:
17.57 g in 1 BOTTLE, GLASS
Product Code:
68605-2002
Proprietary Name:
End-zit
Non-Proprietary Name:
Sulfur
Substance Name:
Sulfur
Usage Information:
Intended for use on blemishes only. This advanced formulation is designed to dry and aid in elimination of pimples. It is make-up quality for excellent coverage of the blemish. It is unbelievably effective, clinically tested, dermatologist approved and recommended.
11-Digit NDC Billing Format:
68605200202
NDC to RxNorm Crosswalk:
  • RxCUI: 1094323 - End-Zit 5 % Topical Lotion
  • RxCUI: 1094323 - sulfur 50 MG/ML Topical Lotion [End-Zit]
  • RxCUI: 1094323 - End-Zit 50 MG/ML Topical Lotion
  • RxCUI: 422938 - sulfur 5 % Topical Lotion
  • RxCUI: 422938 - sulfur 50 MG/ML Topical Lotion
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Abbe Laboratories, Inc.
    Dosage Form:
    Lotion, Augmented - A lotion dosage form that enhances drug delivery. Augmentation does not refer to the strength of the drug in the dosage form. NOTE: CDER has decided to refrain from expanding the use of this dosage form due to difficulties in setting specific criteria that must be met to be considered "augmented".
    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):
  • SULFUR .05 g/g
    • Sample Package:
    No
    FDA Application Number:
    333D
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    04-20-2004
    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 68605-2002-2?

    The NDC Packaged Code 68605-2002-2 is assigned to a package of 17.57 g in 1 bottle, glass of End-zit, a human over the counter drug labeled by Abbe Laboratories, Inc.. The product's dosage form is lotion, augmented and is administered via topical form.

    Is NDC 68605-2002 included in the NDC Directory?

    Yes, End-zit with product code 68605-2002 is active and included in the NDC Directory. The product was first marketed by Abbe Laboratories, Inc. on April 20, 2004 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 68605-2002-2?

    The 11-digit format is 68605200202. 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
    5-4-168605-2002-25-4-268605-2002-02