NDC Package 68210-4164-1 Non-drowsy Daytime Severe Sinus Congestion And Pain

Acetaminophen,Guaifenesin And Phenylephrine Hcl Tablet, Film Coated 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:
68210-4164-1
Package Description:
1 BOTTLE in 1 CARTON / 12 TABLET, FILM COATED in 1 BOTTLE
Product Code:
Proprietary Name:
Non-drowsy Daytime Severe Sinus Congestion And Pain
Non-Proprietary Name:
Acetaminophen, Guaifenesin And Phenylephrine Hcl
Substance Name:
Acetaminophen; Guaifenesin; Phenylephrine Hydrochloride
Usage Information:
Do not take more than directed adults and childrenĀ 12 years and over take 2 caplets every 4 hoursswallow whole - do not crush, chew, or dissolvedo not take more than 10 caplets in 24 hourschildren under 12 years: ask a doctor
11-Digit NDC Billing Format:
68210416401
NDC to RxNorm Crosswalk:
  • RxCUI: 1243679 - acetaminophen 325 MG / guaiFENesin 200 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1243679 - acetaminophen 325 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1243679 - APAP 325 MG / GG 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1243679 - APAP 325 MG / Guaifenesin 200 MG / Phenylephrine Hydrochloride 5 MG Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Spirit Pharmaceuticals Llc
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    M012
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    06-23-2021
    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.

    Frequently Asked Questions

    What is NDC 68210-4164-1?

    The NDC Packaged Code 68210-4164-1 is assigned to a package of 1 bottle in 1 carton / 12 tablet, film coated in 1 bottle of Non-drowsy Daytime Severe Sinus Congestion And Pain, a human over the counter drug labeled by Spirit Pharmaceuticals Llc. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 68210-4164 included in the NDC Directory?

    Yes, Non-drowsy Daytime Severe Sinus Congestion And Pain with product code 68210-4164 is active and included in the NDC Directory. The product was first marketed by Spirit Pharmaceuticals Llc on June 23, 2021 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 68210-4164-1?

    The 11-digit format is 68210416401. 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
    5-4-168210-4164-15-4-268210-4164-01