mucus relief dm
Generic: guaifenesin and dextromethorphan hbr
Labeler: ahold u.s.a., inc,Drug Facts
Product Profile
Brand Name
mucus relief dm
Generic Name
guaifenesin and dextromethorphan hbr
Labeler
ahold u.s.a., inc,
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
dextromethorphan hydrobromide 60 mg/1, guaifenesin 1200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
60000-057
Product ID
60000-057_9c159223-d3f0-48ae-9e4f-f5896838c034
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA206941
Listing Expiration
2026-12-31
Marketing Start
2017-03-17
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60000057
Hyphenated Format
60000-057
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
mucus relief dm (source: ndc)
Generic Name
guaifenesin and dextromethorphan hbr (source: ndc)
Application Number
ANDA206941 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 60 mg/1
- 1200 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (60000-057-65) / 14 TABLET, EXTENDED RELEASE in 1 BOTTLE
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9c159223-d3f0-48ae-9e4f-f5896838c034", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1099074"], "spl_set_id": ["738bbea4-4243-4cbd-980e-a22451b85c4c"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Ahold U.S.A., Inc,"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (60000-057-65) / 14 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "60000-057-65", "marketing_start_date": "20170317"}], "brand_name": "Mucus Relief DM", "product_id": "60000-057_9c159223-d3f0-48ae-9e4f-f5896838c034", "dosage_form": "TABLET, EXTENDED RELEASE", "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": "60000-057", "generic_name": "Guaifenesin and Dextromethorphan HBr", "labeler_name": "Ahold U.S.A., Inc,", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief DM", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "60 mg/1"}, {"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA206941", "marketing_category": "ANDA", "marketing_start_date": "20170317", "listing_expiration_date": "20261231"}