Vicks Dayquil Vapocool Severe Tablet
NDC Package 69423-987-24
Package Information
Vicks Dayquil Vapocool Severe (acetaminophen, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride) tablets is take only as directeddo not exceed 8 caplets per 24 hrsadults & children 12 yrs & over - 2 caplets with water every 4 hrs children 4 to under 12 yrs - ask a doctor children under 4 yrs - do not use. This formulation utilizes a tablet delivery system. Marketed by The Procter & Gamble Manufacturing Company, this product is identified by NDC 69423-987 and is authorized under FDA application M012.
Identification & Billing
- RxCUI: 1110988 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / guaiFENesin 200 MG / phenylephrine HCl 5 MG Oral Tablet
- RxCUI: 1110988 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet
- RxCUI: 1110988 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet
Clinical Specifications
- Adrenergic alpha1-Agonists - [MoA] (Mechanism of Action)
- Decreased Respiratory Secretion Viscosity - [PE] (Physiologic Effect)
- Expectorant - [EPC] (Established Pharmacologic Class)
- Increased Respiratory Secretions - [PE] (Physiologic Effect)
- Sigma-1 Agonist - [EPC] (Established Pharmacologic Class)
- Sigma-1 Receptor Agonists - [MoA] (Mechanism of Action)
- Uncompetitive N-methyl-D-aspartate Receptor Antagonist - [EPC] (Established Pharmacologic Class)
- Uncompetitive NMDA Receptor Antagonists - [MoA] (Mechanism of Action)
- alpha-1 Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
Regulatory & Marketing
Hierarchy Structure
- 69423 - The Procter & Gamble Manufacturing Company
- 69423-987 - Vicks Dayquil Vapocool Severe
- 69423-987-24 - 1 BLISTER PACK in 1 CARTON / 24 TABLET in 1 BLISTER PACK
- 69423-987 - Vicks Dayquil Vapocool Severe
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 69423-987-24 identifies a specific commercial package of 1 blister pack in 1 carton / 24 tablet in 1 blister pack of Vicks Dayquil Vapocool Severe Cold And Flu Plus Congestion, a human over the counter drug labeled by The Procter & Gamble Manufacturing Company. This tablet is formulated for oral use and contains acetaminophen; dextromethorphan hydrobromide; guaifenesin; phenylephrine hydrochloride 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 The Procter & Gamble Manufacturing Company on August 01, 2018. The current certification is valid through December 31, 2026.
How is this The Procter & Gamble Manufacturing Company product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 69423098724. 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.