NDC Package 49580-0813-6 Daytime Nighttime Severe Cold And Flu Relief

View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

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:
49580-0813-6
Package Description:
1 KIT in 1 KIT * 237 mL in 1 BOTTLE * 237 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Daytime Nighttime Severe Cold And Flu Relief
Usage Information:
DAYTIMEtake only as directed (see Overdose warning)do not take more than 4 doses in any 24-hour period measure only with dosing cup provided. Do not use any other dosing device. keep dosing cup with product mL= milliliter adults and children 12 years and over30 mL every 4 hours children 6 to under 12 years 15 mL every 4 hours children 4 to under 6 yearsask a doctor children under 4 years do not use when using other Daytime or Night time products, carefully read each label to ensure correct dosingNIGHTTIMEtake only as directed (see Overdose warning)Do not exceed 4 doses per 24measure only with dosing cup provided. Do not use any other dosing device.   mL= milliliterkeep dosing cup with productadults and children 12 years and over: 30 mL every 4 hourschildren under 12 years of age: do not usewhen using other Daytime or Nighttime products, carefully read each label or ensure correct dosing
11-Digit NDC Billing Format:
49580081306
Labeler Name:
P & L Development, Llc
Sample Package:
No
FDA Application Number:
M012
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
03-26-2021
End Marketing Date:
03-28-2025
Listing Expiration Date:
03-28-2025
Exclude Flag:
D
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.

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Frequently Asked Questions

What is NDC 49580-0813-6?

The NDC Packaged Code 49580-0813-6 is assigned to a package of 1 kit in 1 kit * 237 ml in 1 bottle * 237 ml in 1 bottle of Daytime Nighttime Severe Cold And Flu Relief, labeled by P & L Development, Llc. The product's dosage form is and is administered via form.

Is NDC 49580-0813 included in the NDC Directory?

No, Daytime Nighttime Severe Cold And Flu Relief with product code 49580-0813 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by P & L Development, Llc on March 26, 2021 and its listing in the NDC Directory is set to expire on March 28, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 49580-0813-6?

The 11-digit format is 49580081306. 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 5-4-1 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
5-4-149580-0813-65-4-249580-0813-06