NDC Package 41520-820-90 Careone Day Cold And Flu Night Cold And Flu

View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
41520-820-90
Package Description:
1 KIT in 1 KIT * 8 BLISTER PACK in 1 CARTON / 2 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 4 BLISTER PACK in 1 CARTON / 2 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product Code:
Proprietary Name:
Careone Day Cold And Flu Night Cold And Flu
Usage Information:
•do not take more than directed (see Overdose warning)•do not take more than 10 liquid gels in any 24-hour period•adults and children 12 years of age and older: take 2 liquid gels every 4 hours•children under 12 years of age: do not use
11-Digit NDC Billing Format:
41520082090
NDC to RxNorm Crosswalk:
  • RxCUI: 1110988 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / guaiFENesin 200 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1110988 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1110988 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • 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
  • Labeler Name:
    American Sales Company
    Sample Package:
    No
    Start Marketing Date:
    07-23-2019
    Listing Expiration Date:
    12-31-2022
    Exclude Flag:
    I
    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 41520-820-90?

    The NDC Packaged Code 41520-820-90 is assigned to a package of 1 kit in 1 kit * 8 blister pack in 1 carton / 2 capsule, liquid filled in 1 blister pack * 4 blister pack in 1 carton / 2 capsule, liquid filled in 1 blister pack of Careone Day Cold And Flu Night Cold And Flu, labeled by American Sales Company. The product's dosage form is and is administered via form.

    Is NDC 41520-820 included in the NDC Directory?

    No, Careone Day Cold And Flu Night Cold And Flu with product code 41520-820 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by American Sales Company on July 23, 2019 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 41520-820-90?

    The 11-digit format is 41520082090. 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
    5-3-241520-820-905-4-241520-0820-90