NDC Package 67091-333-18 Tussin Dm Nighttime Cough Maximum Strength

Dextromethorphan Hbr,Doxylamine Succinate 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:
67091-333-18
Package Description:
1 BOTTLE, PLASTIC in 1 BOX / 118 mL in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Tussin Dm Nighttime Cough Maximum Strength
Non-Proprietary Name:
Dextromethorphan Hbr, Doxylamine Succinate
Substance Name:
Dextromethorphan Hydrobromide; Doxylamine Succinate
Usage Information:
This adult product is not intended for use in children under 12 years of age do not take more than 4 doses in any 24-hour period measure only with dosing cup provided. Do not use any other dosing device. keep dosing cup with product mL = milliliter adults and children 12 years and over: 20 mL every 6 hours children under 12 years: do not use
11-Digit NDC Billing Format:
67091033318
NDC to RxNorm Crosswalk:
  • RxCUI: 1115329 - dextromethorphan HBr 30 MG / doxylamine succinate 12.5 MG in 20 mL Oral Solution
  • RxCUI: 1115329 - dextromethorphan hydrobromide 1.5 MG/ML / doxylamine succinate 0.625 MG/ML Oral Solution
  • RxCUI: 1115329 - dextromethorphan hydrobromide 30 MG / doxylamine succinate 12.5 MG per 20 ML Oral Solution
  • RxCUI: 1115329 - dextromethorphan hydrobromide 7.5 MG / doxylamine succinate 3.125 MG per 5 ML Oral Solution
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Winco Foods, 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):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    part341
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    02-01-2019
    End Marketing Date:
    05-31-2024
    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 67091-333-18?

    The NDC Packaged Code 67091-333-18 is assigned to a package of 1 bottle, plastic in 1 box / 118 ml in 1 bottle, plastic of Tussin Dm Nighttime Cough Maximum Strength, a human over the counter drug labeled by Winco Foods, Llc. The product's dosage form is liquid and is administered via oral form.

    Is NDC 67091-333 included in the NDC Directory?

    Yes, Tussin Dm Nighttime Cough Maximum Strength with product code 67091-333 is active and included in the NDC Directory. The product was first marketed by Winco Foods, Llc on February 01, 2019.

    What is the 11-digit format for NDC 67091-333-18?

    The 11-digit format is 67091033318. 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
    5-3-267091-333-185-4-267091-0333-18