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  5. NDC Package Code: 83717-002-01 Wart Removal

NDC Package 83717-002-01 Wart Removal

Wart Removal Liquid Liquid 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:
83717-002-01
Package Description:
15 mL in 1 BOX
Product Code:
83717-002
Proprietary Name:
Wart Removal
Non-Proprietary Name:
Wart Removal Liquid
Substance Name:
Chlorhexidine Acetate; Salicylic Acid
Usage Information:
1 . Wash the corns or warts with warm water2 . Take out the inner plug from the bottle , install the brushinto the bottle cap. press the brush tightly and tighten theca on the bottle3 . Dry the skin , then open the cap , dip the liquid with thebrush and apply it on the wart or com , after the liquid driesand forms to be a mask apply the liquid again . Apply it inthe day and night and twice in each time4 . Applying it for 2 weeks until the skin recovers to ahealthy situation .NOTICE : " lif warts or com are big , you should use it for a longer time . if swallowed , get medical help or contact a poison controlcenter right away
11-Digit NDC Billing Format:
83717000201
Product Type:
Human Otc Drug
Labeler Name:
Wenchang Panzhijie Trading Co., Ltd.
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
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 ACETATE .3 mg/100mL
  • SALICYLIC ACID .3 mg/100mL
    • Pharmacologic Class(es):
  • Decreased Cell Wall Integrity - [PE] (Physiologic Effect)
    • Sample Package:
    No
    FDA Application Number:
    M028
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    10-07-2023
    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 83717-002-01?

    The NDC Packaged Code 83717-002-01 is assigned to a package of 15 ml in 1 box of Wart Removal, a human over the counter drug labeled by Wenchang Panzhijie Trading Co., Ltd.. The product's dosage form is liquid and is administered via topical form.

    Is NDC 83717-002 included in the NDC Directory?

    Yes, Wart Removal with product code 83717-002 is active and included in the NDC Directory. The product was first marketed by Wenchang Panzhijie Trading Co., Ltd. on October 07, 2023 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 83717-002-01?

    The 11-digit format is 83717000201. 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
    5-3-283717-002-015-4-283717-0002-01