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  5. NDC Package Code: 67091-119-18 Childrens Pain Relief Dye-free

NDC Package 67091-119-18 Childrens Pain Relief Dye-free

Acteaminophen Suspension Oral - 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:
67091-119-18
Package Description:
1 BOTTLE in 1 CARTON / 118 mL in 1 BOTTLE
Product Code:
67091-119
Proprietary Name:
Childrens Pain Relief Dye-free
Non-Proprietary Name:
Acteaminophen
Substance Name:
Acetaminophen
Usage Information:
This drug is used to treat mild to moderate pain (from headaches, menstrual periods, toothaches, backaches, osteoarthritis, or cold/flu aches and pains) and to reduce fever.
11-Digit NDC Billing Format:
67091011918
NDC to RxNorm Crosswalk:
  • RxCUI: 307668 - acetaminophen 160 MG in 5 mL Oral Suspension
  • RxCUI: 307668 - acetaminophen 32 MG/ML Oral Suspension
  • RxCUI: 307668 - acetaminophen 160 MG per 5 ML Oral Suspension
  • RxCUI: 307668 - acetaminophen 320 MG per 10 ML Oral Suspension
  • RxCUI: 307668 - acetaminophen 650 MG per 20.3 ML Oral Suspension
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Winco Foods, Llc
    Dosage Form:
    Suspension - A liquid1 dosage form that contains solid particles dispersed in a liquid vehicle.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ACETAMINOPHEN 160 mg/5mL
    • Sample Package:
    No
    FDA Application Number:
    M013
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    12-12-2014
    Listing Expiration Date:
    12-31-2025
    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 67091-119-18?

    The NDC Packaged Code 67091-119-18 is assigned to a package of 1 bottle in 1 carton / 118 ml in 1 bottle of Childrens Pain Relief Dye-free, a human over the counter drug labeled by Winco Foods, Llc. The product's dosage form is suspension and is administered via oral form.

    Is NDC 67091-119 included in the NDC Directory?

    Yes, Childrens Pain Relief Dye-free with product code 67091-119 is active and included in the NDC Directory. The product was first marketed by Winco Foods, Llc on December 12, 2014 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 67091-119-18?

    The 11-digit format is 67091011918. 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
    5-3-267091-119-185-4-267091-0119-18