Daytime Cold And Flu
NDC Package 51013-183-01
Package Information
Daytime Cold And Flu is take only as directed - see Overdose warningdo not exceed 4 doses per 24 hrs adults & children 12 yrs & over 2 softgels with water every 4 hrschildren 4 to under 12 yrs ask a doctorchildren under 4 yrs do not usewhen using other Daytime or Nighttime products, carefully read each label to insure correct dosing. Marketed by Puracap Pharmaceutical Llc, this product is identified by NDC 51013-183 and is authorized under FDA application part341.
Identification & Billing
- RxCUI: 1086997 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG Oral Capsule
- RxCUI: 1086997 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Capsule
- RxCUI: 1086997 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Capsule
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 51013 - Puracap Pharmaceutical Llc
- 51013-183 - Daytime Cold And Flu
- 51013-183-01 - 1 BLISTER PACK in 1 CARTON / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
- 51013-183 - Daytime Cold And Flu
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 full disclaimer at the bottom of this page.
Other Available Packages
The following commercial packages are registered under the same Product NDC (51013-183). Click a package code to view its specific billing and regulatory data.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 51013-183-01 identifies a specific commercial package of 1 blister pack in 1 carton / 10 capsule, liquid filled in 1 blister pack of Daytime Cold And Flu, labeled by Puracap Pharmaceutical Llc. This is formulated for use and contains as the active substance.
Is this product currently listed with the FDA?
This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Puracap Pharmaceutical Llc on October 12, 2016. The current certification is valid through December 31, 2024.
How is this Puracap Pharmaceutical Llc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 51013018301. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.