NDC Package 79903-151-50 Antiseptic

Eucalyptol,Menthol,Methyl Salicylate,Thymol Liquid Oral - 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:
79903-151-50
Package Description:
500 mL in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Antiseptic
Non-Proprietary Name:
Eucalyptol, Menthol, Methyl Salicylate, Thymol
Substance Name:
Eucalyptol; Menthol; Methyl Salicylate; Thymol
Usage Information:
Adults and children 12 years of age and older: vigorously swish 20 milliliters of rinse between your teeth twice a day for 30 seconds and then spit out. Do not swallow the rinse.children 6 years to under 12 years of age: supervise usechildren under 6 years of age: do not use
11-Digit NDC Billing Format:
79903015150
NDC to RxNorm Crosswalk:
  • RxCUI: 1043619 - eucalyptol 0.092 % / menthol 0.042 % / methyl salicylate 0.06 % / thymol 0.064 % Mouthwash
  • RxCUI: 1043619 - eucalyptol 0.92 MG/ML / menthol 0.42 MG/ML / methyl salicylate 0.6 MG/ML / thymol 0.64 MG/ML Mouthwash
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Walmart Inc. (see Also Equate)
    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):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    part356
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    12-30-2022
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    79903-151-751.5 mL in 1 BOTTLE, PLASTIC
    79903-151-992 BOTTLE, PLASTIC in 1 PACKAGE / 1.5 mL in 1 BOTTLE, PLASTIC

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 79903-151-50?

    The NDC Packaged Code 79903-151-50 is assigned to a package of 500 ml in 1 bottle, plastic of Antiseptic, a human over the counter drug labeled by Walmart Inc. (see Also Equate). The product's dosage form is liquid and is administered via oral form.

    Is NDC 79903-151 included in the NDC Directory?

    Yes, Antiseptic with product code 79903-151 is active and included in the NDC Directory. The product was first marketed by Walmart Inc. (see Also Equate) on December 30, 2022 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 79903-151-50?

    The 11-digit format is 79903015150. 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
    5-3-279903-151-505-4-279903-0151-50