mucosa dm
Generic: guaifenesin dextromethorphan
Labeler: time cap laboratories, inc.Drug Facts
Product Profile
Brand Name
mucosa dm
Generic Name
guaifenesin dextromethorphan
Labeler
time cap laboratories, inc.
Dosage Form
TABLET
Routes
Active Ingredients
dextromethorphan hydrobromide 20 mg/1, guaifenesin 400 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
49483-280
Product ID
49483-280_2d9cef2f-22cd-ed8e-e063-6394a90ad8a8
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2012-04-17
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
49483280
Hyphenated Format
49483-280
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
mucosa dm (source: ndc)
Generic Name
guaifenesin dextromethorphan (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
- 400 mg/1
Packaging
- 100000 TABLET in 1 CARTON (49483-280-00)
- 60 TABLET in 1 BOTTLE, PLASTIC (49483-280-06)
- 200 TABLET in 1 BOTTLE (49483-280-20)
Packages (3)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2d9cef2f-22cd-ed8e-e063-6394a90ad8a8", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1147685"], "spl_set_id": ["62c1f4aa-6571-414c-9a58-31e107b7db97"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["TIME CAP LABORATORIES, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100000 TABLET in 1 CARTON (49483-280-00)", "package_ndc": "49483-280-00", "marketing_start_date": "20181217"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (49483-280-06)", "package_ndc": "49483-280-06", "marketing_start_date": "20181217"}, {"sample": false, "description": "200 TABLET in 1 BOTTLE (49483-280-20)", "package_ndc": "49483-280-20", "marketing_start_date": "20230915"}], "brand_name": "MUCOSA DM", "product_id": "49483-280_2d9cef2f-22cd-ed8e-e063-6394a90ad8a8", "dosage_form": "TABLET", "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": "49483-280", "generic_name": "GUAIFENESIN DEXTROMETHORPHAN", "labeler_name": "TIME CAP LABORATORIES, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MUCOSA DM", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/1"}, {"name": "GUAIFENESIN", "strength": "400 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20120417", "listing_expiration_date": "20261231"}