mucus relief congestion and headache maximum strength
Generic: acetaminophen, guaifenesin, phenylephrine hcl
Labeler: dolgencorp, inc. (dollar general & rexall)Drug Facts
Product Profile
Brand Name
mucus relief congestion and headache maximum strength
Generic Name
acetaminophen, guaifenesin, phenylephrine hcl
Labeler
dolgencorp, inc. (dollar general & rexall)
Dosage Form
LIQUID
Routes
Active Ingredients
acetaminophen 650 mg/20mL, guaifenesin 400 mg/20mL, phenylephrine hydrochloride 10 mg/20mL
Manufacturer
Identifiers & Regulatory
Product NDC
55910-757
Product ID
55910-757_c8a19e46-6ec9-40dc-922a-732e1528aadf
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2019-06-01
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55910757
Hyphenated Format
55910-757
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 congestion and headache maximum strength (source: ndc)
Generic Name
acetaminophen, guaifenesin, phenylephrine hcl (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 650 mg/20mL
- 400 mg/20mL
- 10 mg/20mL
Packaging
- 266 mL in 1 BOTTLE, PLASTIC (55910-757-09)
Packages (1)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c8a19e46-6ec9-40dc-922a-732e1528aadf", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0715256702355"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1116568"], "spl_set_id": ["2638b541-e680-4949-a7c7-fcee165cbc92"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "266 mL in 1 BOTTLE, PLASTIC (55910-757-09)", "package_ndc": "55910-757-09", "marketing_start_date": "20190601"}], "brand_name": "Mucus Relief Congestion and Headache Maximum Strength", "product_id": "55910-757_c8a19e46-6ec9-40dc-922a-732e1528aadf", "dosage_form": "LIQUID", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "55910-757", "generic_name": "Acetaminophen, Guaifenesin, Phenylephrine HCL", "labeler_name": "Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief Congestion and Headache", "brand_name_suffix": "Maximum Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 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": "20190601", "listing_expiration_date": "20261231"}