NDC Package 63941-527-08 Severe Sinus Congestion And Pain Non-drowsy, Daytime

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:
63941-527-08
Package Description:
2 BLISTER PACK in 1 CARTON / 12 TABLET, FILM COATED in 1 BLISTER PACK
Product Code:
Proprietary Name:
Severe Sinus Congestion And Pain Non-drowsy, Daytime
Non-Proprietary Name:
Acetaminophen, Guaifenesin And Phenylephrine Hcl
Substance Name:
Acetaminophen; Guaifenesin; Phenylephrine Hydrochloride
Usage Information:
Do not take more than directed adults and children 12 years and overtake 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:
63941052708
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:
    Valu Merchandisers Company
    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:
    08-06-2005
    End Marketing Date:
    08-29-2025
    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.

    Frequently Asked Questions

    What is NDC 63941-527-08?

    The NDC Packaged Code 63941-527-08 is assigned to a package of 2 blister pack in 1 carton / 12 tablet, film coated in 1 blister pack of Severe Sinus Congestion And Pain Non-drowsy, Daytime, a human over the counter drug labeled by Valu Merchandisers Company. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 63941-527 included in the NDC Directory?

    Yes, Severe Sinus Congestion And Pain Non-drowsy, Daytime with product code 63941-527 is active and included in the NDC Directory. The product was first marketed by Valu Merchandisers Company on August 06, 2005.

    What is the 11-digit format for NDC 63941-527-08?

    The 11-digit format is 63941052708. 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
    5-3-263941-527-085-4-263941-0527-08