NDC Package 69842-822-24 Daytime Nighttime Sinus Relief Maximum Strength

Acetaminophen,Dextromethorphan Hbr,Doxylamine Succinate,Phenylephrine Hcl, Guaifenesin Kit - 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:
69842-822-24
Package Description:
1 KIT in 1 KIT * 8 BLISTER PACK in 1 CARTON / 1 CAPSULE in 1 BLISTER PACK * 16 BLISTER PACK in 1 CARTON / 1 CAPSULE in 1 BLISTER PACK
Product Code:
Proprietary Name:
Daytime Nighttime Sinus Relief Maximum Strength
Non-Proprietary Name:
Acetaminophen, Dextromethorphan Hbr, Doxylamine Succinate, Phenylephrine Hcl, Guaifenesin
Usage Information:
DAYTIMEdo not take more than directed (see Overdose warning)do not take more than 12 softgels (Daytime and NightTime) in any 24-hour periodadults and children 12 years of age and older: take 2 softgels every 4 hourschildren under 12 years of age: do not usewhen using other Daytime or Nighttime products, carefully read each label to ensure correct dosingNIGHTTIMEdo not take more than directed (see Overdose warning)do not take more than 12 softgels (Daytime and Nighttime) in any 24-hour periodadults and children 12 years of age and older: take 2 softgels every 4 hourschildren under 12 years of age: do not usewhen using other Daytime or Nighttime products, carefully read each label to ensure correct dosingĀ 
11-Digit NDC Billing Format:
69842082224
NDC to RxNorm Crosswalk:
  • RxCUI: 1297288 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / doxylamine succinate 6.25 MG / phenylephrine HCl 5 MG Oral Capsule
  • RxCUI: 1297288 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / doxylamine succinate 6.25 MG / phenylephrine hydrochloride 5 MG Oral Capsule
  • RxCUI: 1297288 - APAP 325 MG / Dextromethorphan Hydrobromide 10 MG / doxylamine succinate 6.25 MG / Phenylephrine Hydrochloride 5 MG Oral Capsule
  • RxCUI: 1656815 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / guaiFENesin 200 MG / phenylephrine HCl 5 MG Oral Capsule
  • RxCUI: 1656815 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Capsule
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Cvs Pharmacy
    Dosage Form:
    Kit - A packaged collection of related material.
    Sample Package:
    No
    FDA Application Number:
    M012
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    01-31-2019
    End Marketing 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 69842-822-24?

    The NDC Packaged Code 69842-822-24 is assigned to a package of 1 kit in 1 kit * 8 blister pack in 1 carton / 1 capsule in 1 blister pack * 16 blister pack in 1 carton / 1 capsule in 1 blister pack of Daytime Nighttime Sinus Relief Maximum Strength, a human over the counter drug labeled by Cvs Pharmacy. The product's dosage form is kit and is administered via form.

    Is NDC 69842-822 included in the NDC Directory?

    Yes, Daytime Nighttime Sinus Relief Maximum Strength with product code 69842-822 is active and included in the NDC Directory. The product was first marketed by Cvs Pharmacy on January 31, 2019.

    What is the 11-digit format for NDC 69842-822-24?

    The 11-digit format is 69842082224. 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
    5-3-269842-822-245-4-269842-0822-24