mucus relief severe congestion and cough maximum strength

Generic: dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride

Labeler: harris teeter, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief severe congestion and cough maximum strength
Generic Name dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride
Labeler harris teeter, llc
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

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

Manufacturer
Harris Teeter, LLC

Identifiers & Regulatory

Product NDC 69256-337
Product ID 69256-337_bc527934-5f5f-45c2-aa3a-cd1d67dbd61b
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Marketing Start 2021-05-28
Marketing End 2027-05-28

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 69256337
Hyphenated Format 69256-337

Supplemental Identifiers

RxCUI
1043543
UPC
0072036736246
UNII
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 mucus relief severe congestion and cough maximum strength (source: ndc)
Generic Name dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/20mL
  • 400 mg/20mL
  • 10 mg/20mL
source: ndc
Packaging
  • 177 mL in 1 BOTTLE, PLASTIC (69256-337-06)
source: ndc

Packages (1)

69256-337-06 177 mL in 1 BOTTLE, PLASTIC (69256-337-06)

Ingredients (3)

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

Linked Drug Pages (1)

Mucus Relief Severe Congestion and Cough Maximum Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "bc527934-5f5f-45c2-aa3a-cd1d67dbd61b", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0072036736246"], "unii": ["9D2RTI9KYH", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1043543"], "spl_set_id": ["e0a62fa1-9f8a-4770-b28b-1f4f02a762e0"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Harris Teeter, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "177 mL in 1 BOTTLE, PLASTIC (69256-337-06)", "package_ndc": "69256-337-06", "marketing_end_date": "20270528", "marketing_start_date": "20210528"}], "brand_name": "Mucus Relief Severe Congestion and Cough Maximum Strength", "product_id": "69256-337_bc527934-5f5f-45c2-aa3a-cd1d67dbd61b", "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": "69256-337", "generic_name": "Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride", "labeler_name": "Harris Teeter, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief Severe Congestion and Cough", "brand_name_suffix": "Maximum Strength", "active_ingredients": [{"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_end_date": "20270528", "marketing_start_date": "20210528"}