NDC Package 73006-108-41 Only For Cold And Flu Cough Suppressant

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:
73006-108-41
Package Description:
1 BLISTER PACK in 1 CARTON / 4 TABLET in 1 BLISTER PACK
Product Code:
Proprietary Name:
Only For Cold And Flu Cough Suppressant
Usage Information:
Do not take more than directed - See Overdose warningtake with a full glass of water • do not exceed 8 caplets per 24 hours adults and children 12 yrs of age & over2 caplets with water every 4 hrs  children 4 to 12 years of ageask a doctor children under 4 years of agedo not usewhen using other Daytime or Night time products, carefully read each label to ensure correct dosing
11-Digit NDC Billing Format:
73006010841
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
  • Labeler Name:
    O4 Global Trading Usa, Llc
    Sample Package:
    No
    Start Marketing Date:
    02-01-2019
    Listing Expiration Date:
    12-31-2021
    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 73006-108-41?

    The NDC Packaged Code 73006-108-41 is assigned to a package of 1 blister pack in 1 carton / 4 tablet in 1 blister pack of Only For Cold And Flu Cough Suppressant, labeled by O4 Global Trading Usa, Llc. The product's dosage form is and is administered via form.

    Is NDC 73006-108 included in the NDC Directory?

    No, Only For Cold And Flu Cough Suppressant with product code 73006-108 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by O4 Global Trading Usa, Llc on February 01, 2019 and its listing in the NDC Directory is set to expire on December 31, 2021 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 73006-108-41?

    The 11-digit format is 73006010841. 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
    5-3-273006-108-415-4-273006-0108-41