mucus relief dm
Generic: dextromethorphan hbr, guaifenesin
Labeler: cardinal health 110, llc. dba leaderDrug Facts
Product Profile
Brand Name
mucus relief dm
Generic Name
dextromethorphan hbr, guaifenesin
Labeler
cardinal health 110, llc. dba leader
Dosage Form
SOLUTION
Routes
Active Ingredients
dextromethorphan hydrobromide 20 mg/20mL, guaifenesin 400 mg/20mL
Manufacturer
Identifiers & Regulatory
Product NDC
70000-0707
Product ID
70000-0707_58d92ad8-bd35-4512-84d6-23c4ea41a9c6
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2024-09-24
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
700000707
Hyphenated Format
70000-0707
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 (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 (70000-0707-1)
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "58d92ad8-bd35-4512-84d6-23c4ea41a9c6", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0096295144369"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1020138"], "spl_set_id": ["4136e5f4-cc00-46d6-aa7f-ef56d087d7ec"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Cardinal Health 110, LLC. DBA Leader"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "177 mL in 1 BOTTLE, PLASTIC (70000-0707-1)", "package_ndc": "70000-0707-1", "marketing_start_date": "20240924"}], "brand_name": "Mucus Relief DM", "product_id": "70000-0707_58d92ad8-bd35-4512-84d6-23c4ea41a9c6", "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": "70000-0707", "generic_name": "Dextromethorphan HBr, Guaifenesin", "labeler_name": "Cardinal Health 110, LLC. DBA Leader", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief DM", "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": "20240924", "listing_expiration_date": "20261231"}