meijer mucus relief dm maximum strength
Generic: dextromethorphan hbr and guaifenesin
Labeler: meijer, inc.Drug Facts
Product Profile
Brand Name
meijer mucus relief dm maximum strength
Generic Name
dextromethorphan hbr and guaifenesin
Labeler
meijer, inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
dextromethorphan hydrobromide 20 mg/20mL, guaifenesin 400 mg/20mL
Manufacturer
Identifiers & Regulatory
Product NDC
41250-748
Product ID
41250-748_41f35ef0-a662-adaa-e063-6294a90a3d3b
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2020-04-20
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
41250748
Hyphenated Format
41250-748
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
meijer mucus relief dm maximum strength (source: ndc)
Generic Name
dextromethorphan hbr and guaifenesin (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/20mL
- 400 mg/20mL
Packaging
- 180 mL in 1 BOTTLE (41250-748-06)
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "41f35ef0-a662-adaa-e063-6294a90a3d3b", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1020138"], "spl_set_id": ["12cbe71a-a796-4f14-848e-aa6082dac032"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["MEIJER, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "180 mL in 1 BOTTLE (41250-748-06)", "package_ndc": "41250-748-06", "marketing_start_date": "20200420"}], "brand_name": "Meijer Mucus Relief DM Maximum Strength", "product_id": "41250-748_41f35ef0-a662-adaa-e063-6294a90a3d3b", "dosage_form": "SOLUTION", "pharm_class": ["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]"], "product_ndc": "41250-748", "generic_name": "Dextromethorphan HBr and Guaifenesin", "labeler_name": "MEIJER, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Meijer Mucus Relief DM", "brand_name_suffix": "Maximum Strength", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/20mL"}, {"name": "GUAIFENESIN", "strength": "400 mg/20mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200420", "listing_expiration_date": "20261231"}