69842-767 NDC - CVS MAXIMUM STRENGTH SEVERE CONGESTION AND COUGH (DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE)

Drug Information

  • Product NDC: 69842-767
  • Proprietary Name: CVS Maximum Strength Severe Congestion and Cough
  • Non Proprietary Name: dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride
  • Active Ingredient(s): 20 mg/20mL DEXTROMETHORPHAN HYDROBROMIDE; 400 mg/20mL GUAIFENESIN; 10 mg/20mL PHENYLEPHRINE HYDROCHLORIDE
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Adrenergic alpha1-Agonists [MoA]; Decreased Respiratory Secretion Viscosity [PE]; Expectorant [EPC]; Increased Respiratory Secretions [PE]; Sigma-1 Agonist [EPC]; Sigma-1 Receptor Agonists [MoA]; Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]; Uncompetitive NMDA Receptor Antagonists [MoA]; alpha-1 Adrenergic Agonist [EPC]

Labeler Information

Field Name Field Value
Labeler Name: CVS PHARMACY, INC
Product Type: HUMAN OTC DRUG
FDA Application Number: M012
Marketing Category: OTC MONOGRAPH DRUG
Start Marketing Date:3/31/2020

Package Information

No. Package Code Package Description Billing Unit
169842-767-06180 mL in 1 BOTTLE, PLASTIC (69842-767-06)

NDC Record

Field Name Field Value Definition
PRODUCT NDC69842-767The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMECVS Maximum Strength Severe Congestion and CoughThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEdextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochlorideThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE3/31/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
APPLICATION NUMBERM012The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
LABELER NAMECVS PHARMACY, INCThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
SUBSTANCE NAMEDEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDEThe translation of the dosage form Code submitted by the firm.
ACTIVE NUMERATOR STRENGTH20; 400; 10The translation of the route code submitted by the firm, indicating route of administration.
ACTIVE INGRED UNITmg/20mL; mg/20mL; mg/20mL 
PHARM CLASSESAdrenergic alpha1-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA], alpha-1 Adrenergic Agonist [EPC] 

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This page was last updated on: 11/21/2025

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