mucus relief dm max maximum strength
Generic: dextromethorphan hbr, guaifenesin
Labeler: top care (topco associates llc)Drug Facts
Product Profile
Brand Name
mucus relief dm max maximum strength
Generic Name
dextromethorphan hbr, guaifenesin
Labeler
top care (topco associates llc)
Dosage Form
LIQUID
Routes
Active Ingredients
dextromethorphan hydrobromide 20 mg/20mL, guaifenesin 400 mg/20mL
Manufacturer
Identifiers & Regulatory
Product NDC
36800-605
Product ID
36800-605_b0015f7d-7eb0-4a76-a83d-85576051d9c7
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2016-04-30
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
36800605
Hyphenated Format
36800-605
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 dm max maximum strength (source: ndc)
Generic Name
dextromethorphan hbr, guaifenesin (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/20mL
- 400 mg/20mL
Packaging
- 177 mL in 1 BOTTLE, PLASTIC (36800-605-06)
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b0015f7d-7eb0-4a76-a83d-85576051d9c7", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0036800386174"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1020138"], "spl_set_id": ["aa1eb90c-e565-455f-8978-6f2f9e00a814"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["TOP CARE (Topco Associates LLC)"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "177 mL in 1 BOTTLE, PLASTIC (36800-605-06)", "package_ndc": "36800-605-06", "marketing_start_date": "20160430"}], "brand_name": "Mucus Relief DM Max Maximum Strength", "product_id": "36800-605_b0015f7d-7eb0-4a76-a83d-85576051d9c7", "dosage_form": "LIQUID", "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": "36800-605", "generic_name": "Dextromethorphan HBr, Guaifenesin", "labeler_name": "TOP CARE (Topco Associates LLC)", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief DM Max", "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": "20160430", "listing_expiration_date": "20261231"}