1. Home
  2. Labeler Index
  3. Select Brand Dist.
  4. 15127-923
  5. NDC Package Code: 15127-923-08 Flu Relief Therapy Daytime Severe Cold

NDC Package 15127-923-08 Flu Relief Therapy Daytime Severe Cold

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
15127-923-08
Package Description:
237 LIQUID in 1 BOTTLE, PLASTIC
Product Code:
15127-923
Proprietary Name:
Flu Relief Therapy Daytime Severe Cold
Usage Information:
Do not use in infants do not exceed recommended dose (see overdose warning) use dosage cup providedtbsp = tablespoon, mL = milliliteragedose adults and children 12 years and over 2 tablespoons (30 mL) every 4 hours  children 4 to 11 years do not use unless directed by a doctor children under 4 years do not useDo not take more than 6 doses (12 tablespoons) in 24 hours.
11-Digit NDC Billing Format:
15127092308
NDC to RxNorm Crosswalk:
  • RxCUI: 1113705 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG in 15 mL Oral Solution
  • RxCUI: 1113705 - acetaminophen 21.7 MG/ML / dextromethorphan hydrobromide 0.667 MG/ML / phenylephrine hydrochloride 0.333 MG/ML Oral Solution
  • RxCUI: 1113705 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG per 15 ML Oral Solution
  • RxCUI: 1113705 - acetaminophen 650 MG / dextromethorphan HBr 20 MG / phenylephrine HCl 10 MG per 30 ML Oral Solution
  • RxCUI: 1113705 - APAP 21.7 MG/ML / dextromethorphan hydrobromide 0.667 MG/ML / phenylephrine hydrochloride 0.333 MG/ML Oral Solution
    • Labeler Name:
    Select Brand Dist.
    Sample Package:
    No
    Start Marketing Date:
    08-22-2007
    Listing Expiration Date:
    12-31-2019
    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 15127-923-08?

    The NDC Packaged Code 15127-923-08 is assigned to a package of 237 liquid in 1 bottle, plastic of Flu Relief Therapy Daytime Severe Cold, labeled by Select Brand Dist.. The product's dosage form is and is administered via form.

    Is NDC 15127-923 included in the NDC Directory?

    No, Flu Relief Therapy Daytime Severe Cold with product code 15127-923 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Select Brand Dist. on August 22, 2007 and its listing in the NDC Directory is set to expire on December 31, 2019 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 15127-923-08?

    The 11-digit format is 15127092308. 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
    5-3-215127-923-085-4-215127-0923-08