mucus relief sinus severe congestion relief
Generic: acetaminophen, guaifenesin, and phenylephrine hydrochloride
Labeler: chain drug consortiumDrug Facts
Product Profile
Brand Name
mucus relief sinus severe congestion relief
Generic Name
acetaminophen, guaifenesin, and phenylephrine hydrochloride
Labeler
chain drug consortium
Dosage Form
TABLET, COATED
Routes
Active Ingredients
acetaminophen 325 mg/1, guaifenesin 200 mg/1, phenylephrine hydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68016-549
Product ID
68016-549_2433f431-a224-8a70-e063-6294a90ae450
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Marketing Start
2014-09-01
Marketing End
2026-07-31
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68016549
Hyphenated Format
68016-549
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 sinus severe congestion relief (source: ndc)
Generic Name
acetaminophen, guaifenesin, and phenylephrine hydrochloride (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 325 mg/1
- 200 mg/1
- 5 mg/1
Packaging
- 2 BLISTER PACK in 1 CARTON (68016-549-20) / 10 TABLET, COATED in 1 BLISTER PACK
Packages (1)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2433f431-a224-8a70-e063-6294a90ae450", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0840986030994"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["e0c7ea4d-8a6e-4647-9a8d-dae44ae4a3af"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["CHAIN DRUG CONSORTIUM"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (68016-549-20) / 10 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "68016-549-20", "marketing_end_date": "20260731", "marketing_start_date": "20140901"}], "brand_name": "Mucus Relief Sinus Severe Congestion Relief", "product_id": "68016-549_2433f431-a224-8a70-e063-6294a90ae450", "dosage_form": "TABLET, COATED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "68016-549", "generic_name": "ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "CHAIN DRUG CONSORTIUM", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief Sinus Severe Congestion Relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "GUAIFENESIN", "strength": "200 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20260731", "marketing_start_date": "20140901"}