cvs maximum strength cold and flu relief

Generic: acetaminophen, dextromethorphan hydrobromide, guaifenesin ,phenylephrine hcl

Labeler: cvs pharmacy
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name cvs maximum strength cold and flu relief
Generic Name acetaminophen, dextromethorphan hydrobromide, guaifenesin ,phenylephrine hcl
Labeler cvs pharmacy
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/20mL, dextromethorphan hydrobromide 20 mg/20mL, guaifenesin 400 mg/20mL, phenylephrine hydrochloride 10 mg/20mL

Manufacturer
CVS PHARMACY

Identifiers & Regulatory

Product NDC 69842-903
Product ID 69842-903_4596c422-6c26-b3f1-e063-6394a90aa497
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2021-02-10

Pharmacologic Class

Established (EPC)
expectorant [epc]
Physiologic Effect
decreased respiratory secretion viscosity [pe] increased respiratory secretions [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69842903
Hyphenated Format 69842-903

Supplemental Identifiers

RxCUI
1116572
UNII
362O9ITL9D 9D2RTI9KYH 495W7451VQ 04JA59TNSJ
NUI
N0000193956 N0000008867 N0000009560

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name cvs maximum strength cold and flu relief (source: ndc)
Generic Name acetaminophen, dextromethorphan hydrobromide, guaifenesin ,phenylephrine hcl (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/20mL
  • 20 mg/20mL
  • 400 mg/20mL
  • 10 mg/20mL
source: ndc
Packaging
  • 180 mL in 1 BOTTLE, PLASTIC (69842-903-06)
  • 266 mL in 1 BOTTLE, PLASTIC (69842-903-09)
source: ndc

Packages (2)

Ingredients (4)

acetaminophen (650 mg/20mL) dextromethorphan hydrobromide (20 mg/20mL) guaifenesin (400 mg/20mL) phenylephrine hydrochloride (10 mg/20mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4596c422-6c26-b3f1-e063-6394a90aa497", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1116572"], "spl_set_id": ["e1c246a4-7a8c-4761-ab26-13b5165029cc"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["CVS PHARMACY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "180 mL in 1 BOTTLE, PLASTIC (69842-903-06)", "package_ndc": "69842-903-06", "marketing_start_date": "20210210"}, {"sample": false, "description": "266 mL in 1 BOTTLE, PLASTIC (69842-903-09)", "package_ndc": "69842-903-09", "marketing_start_date": "20210210"}], "brand_name": "CVS Maximum Strength Cold and Flu Relief", "product_id": "69842-903_4596c422-6c26-b3f1-e063-6394a90aa497", "dosage_form": "LIQUID", "pharm_class": ["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]"], "product_ndc": "69842-903", "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin ,Phenylephrine HCL", "labeler_name": "CVS PHARMACY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "CVS Maximum Strength Cold and Flu Relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/20mL"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/20mL"}, {"name": "GUAIFENESIN", "strength": "400 mg/20mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/20mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210210", "listing_expiration_date": "20261231"}