mucus relief dm
Generic: dextromethorphan hydrobromide guaifenesin
Labeler: the kroger co.Drug Facts
Product Profile
Brand Name
mucus relief dm
Generic Name
dextromethorphan hydrobromide guaifenesin
Labeler
the kroger co.
Dosage Form
LIQUID
Routes
Active Ingredients
dextromethorphan hydrobromide 20 mg/20mL, guaifenesin 400 mg/20mL
Manufacturer
Identifiers & Regulatory
Product NDC
30142-508
Product ID
30142-508_0c406a49-c216-42e9-a27e-da662dd71d2d
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2020-09-01
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
30142508
Hyphenated Format
30142-508
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 hydrobromide 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 (30142-508-06)
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0c406a49-c216-42e9-a27e-da662dd71d2d", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0041260010828"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1020138"], "spl_set_id": ["49829083-5c0a-4620-bfb3-7103642368db"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["The Kroger Co."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "177 mL in 1 BOTTLE, PLASTIC (30142-508-06)", "package_ndc": "30142-508-06", "marketing_start_date": "20200901"}], "brand_name": "Mucus Relief DM", "product_id": "30142-508_0c406a49-c216-42e9-a27e-da662dd71d2d", "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": "30142-508", "generic_name": "Dextromethorphan Hydrobromide Guaifenesin", "labeler_name": "The Kroger Co.", "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": "20200901", "listing_expiration_date": "20261231"}