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  5. NDC Package Code: 80514-004-01 Pre-moistened Towelette

NDC Package 80514-004-01 Pre-moistened Towelette

Chlorhexidine Gluconate Swab 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:
80514-004-01
Package Description:
1.2 g in 1 POUCH
Product Code:
80514-004
Proprietary Name:
Pre-moistened Towelette
Non-Proprietary Name:
Chlorhexidine Gluconate
Substance Name:
Chlorhexidine Gluconate
Usage Information:
This medication is used along with regular tooth brushing/flossing to treat gingivitis, a gum disease that causes red, swollen, and easily bleeding gums. Chlorhexidine belongs to a class of drugs known as antimicrobials. It works by decreasing the amount of bacteria in the mouth, helping to reduce swelling and redness of the gums and bleeding when you brush.
11-Digit NDC Billing Format:
80514000401
NDC to RxNorm Crosswalk:
  • RxCUI: 2289028 - chlorhexidine acetate 0.2 % Medicated Pad
  • RxCUI: 2289028 - chlorhexidine acetate 2 MG/ML Medicated Pad
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Jiangsu Haida International Trading Co., Ltd.
    Dosage Form:
    Swab - A small piece of relatively flat absorbent material that contains a drug. A swab may also be attached to one end of a small stick. A swab is typically used for applying medication or for cleansing.
    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):
  • CHLORHEXIDINE GLUCONATE .2 g/100g
    • Pharmacologic Class(es):
  • Decreased Cell Wall Integrity - [PE] (Physiologic Effect)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date:
    09-04-2020
    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 80514-004-01?

    The NDC Packaged Code 80514-004-01 is assigned to a package of 1.2 g in 1 pouch of Pre-moistened Towelette, a human over the counter drug labeled by Jiangsu Haida International Trading Co., Ltd.. The product's dosage form is swab and is administered via topical form.

    Is NDC 80514-004 included in the NDC Directory?

    Yes, Pre-moistened Towelette with product code 80514-004 is active and included in the NDC Directory. The product was first marketed by Jiangsu Haida International Trading Co., Ltd. on September 04, 2020 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 80514-004-01?

    The 11-digit format is 80514000401. 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
    5-3-280514-004-015-4-280514-0004-01