Maximum Strength Daytime Cold And Flu And Nighttime Severe Cold And Flu Kit
NDC Package 11673-286-01
Package Information
Maximum Strength Daytime Cold And Flu And Nighttime Severe Cold And Flu (acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, and acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride, triprolidine hydrochloride) kits is a medication used as Active ingredients (in each 20 mL) MUCINEX FAST-MAX COLD & FLU PurposesAcetaminophen 650 mgPain reliever/fever reducerDextromethorphan HBr 20 mgCough suppressantGuaifenesin 400 mgExpectorantPhenylephrine HCl 10 mgNasal decongestantActive ingredients (in each 20 mL) MUCINEX NIGHTSHIFT SEVERE COLD & FLU PurposesAcetaminophen 650 mgPain reliever/fever reducerDextromethorphan HBr 20 mgCough suppressantPhenylephrine HCl 10 mgNasal decongestantTriprolidine HCl 2.5 mgAntihistamine. This formulation utilizes a kit delivery system. Marketed by Target Corporation, this product is identified by NDC 11673-286 and is authorized under FDA application M012.
Identification & Billing
- RxCUI: 1116572 - acetaminophen 650 MG / dextromethorphan HBr 20 MG / guaiFENesin 400 MG / phenylephrine HCl 10 MG in 20 mL Oral Solution
- RxCUI: 1116572 - acetaminophen 32.5 MG/ML / dextromethorphan hydrobromide 1 MG/ML / guaifenesin 20 MG/ML / phenylephrine hydrochloride 0.5 MG/ML Oral Solution
- RxCUI: 1116572 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG per 10 ML Oral Solution
- RxCUI: 1116572 - acetaminophen 650 MG / dextromethorphan HBr 20 MG / guaifenesin 400 MG / phenylephrine hydrochloride 10 MG per 20 ML Oral Solution
- RxCUI: 1116572 - APAP 32.5 MG/ML / Dextromethorphan Hydrobromide 1 MG/ML / Guaifenesin 20 MG/ML / Phenylephrine Hydrochloride 0.5 MG/ML Oral Solution
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 11673 - Target Corporation
- 11673-286 - Maximum Strength Daytime Cold And Flu And Nighttime Severe Cold And Flu
- 11673-286-01 - 1 KIT in 1 CARTON * 180 mL in 1 BOTTLE (11673-872-03) * 180 mL in 1 BOTTLE (11673-295-03)
- 11673-286 - Maximum Strength Daytime Cold And Flu And Nighttime Severe 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.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 11673-286-01 identifies a specific commercial package of 1 kit in 1 carton * 180 ml in 1 bottle (11673-872-03) * 180 ml in 1 bottle (11673-295-03) of Maximum Strength Daytime Cold And Flu And Nighttime Severe Cold And Flu, a human over the counter drug labeled by Target Corporation. This kit is formulated for use and contains as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Target Corporation on May 01, 2024. The current certification is valid through December 31, 2026.
How is this Target Corporation product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 11673028601. 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.
