NDC Package 17856-0045-1 Max Relief Junior

Acetaminophen 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:
17856-0045-1
Package Description:
48 SYRINGE in 1 BOX, UNIT-DOSE / 7.5 mL in 1 SYRINGE (17856-0045-5)
Product Code:
Proprietary Name:
Max Relief Junior
Non-Proprietary Name:
Acetaminophen
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:
17856004501
NDC to RxNorm Crosswalk:
  • RxCUI: 307675 - acetaminophen 160 MG in 5 mL Oral Solution
  • RxCUI: 307675 - acetaminophen 32 MG/ML Oral Solution
  • RxCUI: 307675 - acetaminophen 160 MG per 5 ML Oral Solution
  • RxCUI: 307675 - acetaminophen 325 MG per 10.15 ML Oral Solution
  • RxCUI: 307675 - acetaminophen 650 MG per 20.3 ML Oral Solution
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Atlantic Biologicals Corp.
    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.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    M
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    05-14-2023
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    17856-0045-2120 SYRINGE in 1 BOX, UNIT-DOSE / 1.25 mL in 1 SYRINGE (17856-0045-6)
    17856-0045-3120 SYRINGE in 1 BOX, UNIT-DOSE / 2.5 mL in 1 SYRINGE (17856-0045-7)
    17856-0045-4120 SYRINGE in 1 BOX, UNIT-DOSE / 2.5 mL in 1 SYRINGE (17856-0045-8)

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 17856-0045-1?

    The NDC Packaged Code 17856-0045-1 is assigned to a package of 48 syringe in 1 box, unit-dose / 7.5 ml in 1 syringe (17856-0045-5) of Max Relief Junior, a human over the counter drug labeled by Atlantic Biologicals Corp.. The product's dosage form is liquid and is administered via oral form.

    Is NDC 17856-0045 included in the NDC Directory?

    Yes, Max Relief Junior with product code 17856-0045 is active and included in the NDC Directory. The product was first marketed by Atlantic Biologicals Corp. on May 14, 2023 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 17856-0045-1?

    The 11-digit format is 17856004501. 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 5-4-1 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
    5-4-117856-0045-15-4-217856-0045-01