mucus relief cold flu and sore throat maximum strength
Generic: acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl
Labeler: quality choice (chain drug marketing association)Drug Facts
Product Profile
Brand Name
mucus relief cold flu and sore throat maximum strength
Generic Name
acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl
Labeler
quality choice (chain drug marketing association)
Dosage Form
LIQUID
Routes
Active Ingredients
acetaminophen 650 mg/20mL, dextromethorphan hydrobromide 20 mg/20mL, guaifenesin 400 mg/20mL, phenylephrine hydrochloride 10 mg/20mL
Manufacturer
Identifiers & Regulatory
Product NDC
63868-746
Product ID
63868-746_4b106ebe-59cb-4ff2-8cd8-0a24f8fabc92
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2015-01-31
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63868746
Hyphenated Format
63868-746
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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 cold flu and sore throat maximum strength (source: ndc)
Generic Name
acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 650 mg/20mL
- 20 mg/20mL
- 400 mg/20mL
- 10 mg/20mL
Packaging
- 177 mL in 1 BOTTLE, PLASTIC (63868-746-07)
Packages (1)
Ingredients (4)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4b106ebe-59cb-4ff2-8cd8-0a24f8fabc92", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0635515970199"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1116572"], "spl_set_id": ["bca87923-76cb-446b-a6f7-4e01f6672ccc"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["QUALITY CHOICE (Chain Drug Marketing Association)"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "177 mL in 1 BOTTLE, PLASTIC (63868-746-07)", "package_ndc": "63868-746-07", "marketing_start_date": "20150131"}], "brand_name": "Mucus Relief Cold Flu and Sore Throat Maximum Strength", "product_id": "63868-746_4b106ebe-59cb-4ff2-8cd8-0a24f8fabc92", "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": "63868-746", "generic_name": "Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl", "labeler_name": "QUALITY CHOICE (Chain Drug Marketing Association)", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief Cold Flu and Sore Throat", "brand_name_suffix": "Maximum Strength", "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": "20150131", "listing_expiration_date": "20261231"}