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  5. NDC Package Code: 55316-318-69 Antiseptic

NDC Package 55316-318-69 Antiseptic

Eucalyptol,Menthol,Methyl Salicylate,Thymol Rinse Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
55316-318-69
Package Description:
250 mL in 1 BOTTLE, PLASTIC
Product Code:
55316-318
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 mL (2/3 FL OZ or 4 teaspoonfuls) between teeth for 30 seconds then spit out; do not swallowchildren under 12 years of age consult a dentist or doctorthis rinse is not intended to replace brushing or flossing
11-Digit NDC Billing Format:
55316031869
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:
    Dza Brands, Llc
    Dosage Form:
    Rinse - A liquid used to cleanse by flushing.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • EUCALYPTOL .92 mg/mL
  • MENTHOL .42 mg/mL
  • METHYL SALICYLATE .6 mg/mL
  • THYMOL .64 mg/mL
    • 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:
    02-05-2008
    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
    55316-318-861000 mL in 1 BOTTLE, PLASTIC

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 55316-318-69?

    The NDC Packaged Code 55316-318-69 is assigned to a package of 250 ml in 1 bottle, plastic of Antiseptic, a human over the counter drug labeled by Dza Brands, Llc. The product's dosage form is rinse and is administered via oral form.

    Is NDC 55316-318 included in the NDC Directory?

    Yes, Antiseptic with product code 55316-318 is active and included in the NDC Directory. The product was first marketed by Dza Brands, Llc on February 05, 2008 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 55316-318-69?

    The 11-digit format is 55316031869. 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
    5-3-255316-318-695-4-255316-0318-69