NDC Package 83176-008-01 Dr. Luke Molluscum Wart Remover

Molluscum Wart Remover Liquid 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:
83176-008-01
Package Description:
15 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Dr. Luke Molluscum Wart Remover
Non-Proprietary Name:
Molluscum Wart Remover
Substance Name:
Chlorhexidine; Salicylic Acid
Usage Information:
1. Wash wart and surrounding skin with rubbing alcohol orastringent solution (e.g.: Potassium Permanganate solution), anddry the area thoroughly. 2. Apply a small amount of liquid solution onto the wart with acotton swab, and press the wart 2-3 times. Avoid applying onhealthy skin. 3. Do not apply the liquid over 1 ml onto the affected area. Afterapplying, let the affected area dry. 4. Use once in the morning and evening continuously for 7 daysThe wart will begin to fall off after the last day of treatment. stopusing, and observe for 3 days.Repeat the treatment p rocess if the wart has not yet fallen off.lf swallowed,rinse immediately with water, and get medicalhelp or contact a poison control center right away
11-Digit NDC Billing Format:
83176000801
Product Type:
Human Otc Drug
Labeler Name:
Dr.luke Healthcare Llc
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.
  • Sample Package:
    No
    FDA Application Number:
    M028
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    04-17-2023
    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 83176-008-01?

    The NDC Packaged Code 83176-008-01 is assigned to a package of 15 ml in 1 bottle of Dr. Luke Molluscum Wart Remover, a human over the counter drug labeled by Dr.luke Healthcare Llc. The product's dosage form is liquid and is administered via topical form.

    Is NDC 83176-008 included in the NDC Directory?

    Yes, Dr. Luke Molluscum Wart Remover with product code 83176-008 is active and included in the NDC Directory. The product was first marketed by Dr.luke Healthcare Llc on April 17, 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 83176-008-01?

    The 11-digit format is 83176000801. 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
    5-3-283176-008-015-4-283176-0008-01