maximum strength mucus relief severe congestion and cough
Generic: dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride
Labeler: supervalu inc.,Drug Facts
Product Profile
Brand Name
maximum strength mucus relief severe congestion and cough
Generic Name
dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride
Labeler
supervalu inc.,
Dosage Form
LIQUID
Routes
Active Ingredients
dextromethorphan hydrobromide 20 mg/20mL, guaifenesin 400 mg/20mL, phenylephrine hydrochloride 10 mg/20mL
Manufacturer
Identifiers & Regulatory
Product NDC
41163-738
Product ID
41163-738_3bb76952-15d8-4a36-a392-60f62b845f09
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH FINAL
Application Number
part341
Listing Expiration
2026-12-31
Marketing Start
2017-09-07
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
41163738
Hyphenated Format
41163-738
Supplemental Identifiers
RxCUI
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
maximum strength mucus relief severe congestion and cough (source: ndc)
Generic Name
dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride (source: ndc)
Application Number
part341 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/20mL
- 400 mg/20mL
- 10 mg/20mL
Packaging
- 180 mL in 1 BOTTLE (41163-738-06)
Packages (1)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3bb76952-15d8-4a36-a392-60f62b845f09", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1043543"], "spl_set_id": ["3bb76952-15d8-4a36-a392-60f62b845f09"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["SuperValu Inc.,"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "180 mL in 1 BOTTLE (41163-738-06)", "package_ndc": "41163-738-06", "marketing_start_date": "20170907"}], "brand_name": "maximum strength mucus relief severe congestion and cough", "product_id": "41163-738_3bb76952-15d8-4a36-a392-60f62b845f09", "dosage_form": "LIQUID", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "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": "41163-738", "generic_name": "dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride", "labeler_name": "SuperValu Inc.,", "product_type": "HUMAN OTC DRUG", "brand_name_base": "maximum strength mucus relief severe congestion and cough", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/20mL"}, {"name": "GUAIFENESIN", "strength": "400 mg/20mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/20mL"}], "application_number": "part341", "marketing_category": "OTC MONOGRAPH FINAL", "marketing_start_date": "20170907", "listing_expiration_date": "20261231"}