mucus relief dm immediate release
Generic: mucus relief dm
Labeler: allegiant healthDrug Facts
Product Profile
Brand Name
mucus relief dm immediate release
Generic Name
mucus relief dm
Labeler
allegiant health
Dosage Form
TABLET
Routes
Active Ingredients
dextromethorphan hydrobromide 20 mg/1, guaifenesin 400 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
69168-432
Product ID
69168-432_751cf188-7b5f-4f9d-ba3e-8ce7997ecd31
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2022-05-18
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69168432
Hyphenated Format
69168-432
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 immediate release (source: ndc)
Generic Name
mucus relief dm (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
- 400 mg/1
Packaging
- 120 TABLET in 1 BOTTLE (69168-432-06)
- 1 BOTTLE in 1 CARTON (69168-432-07) / 10 TABLET in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (69168-432-26) / 20 TABLET in 1 BOTTLE
- 30 TABLET in 1 BOTTLE (69168-432-30)
- 50 TABLET in 1 BOTTLE (69168-432-50)
- 200 TABLET in 1 BOTTLE (69168-432-98)
Packages (6)
69168-432-06
120 TABLET in 1 BOTTLE (69168-432-06)
69168-432-07
1 BOTTLE in 1 CARTON (69168-432-07) / 10 TABLET in 1 BOTTLE
69168-432-26
1 BOTTLE in 1 CARTON (69168-432-26) / 20 TABLET in 1 BOTTLE
69168-432-30
30 TABLET in 1 BOTTLE (69168-432-30)
69168-432-50
50 TABLET in 1 BOTTLE (69168-432-50)
69168-432-98
200 TABLET in 1 BOTTLE (69168-432-98)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "751cf188-7b5f-4f9d-ba3e-8ce7997ecd31", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1147685"], "spl_set_id": ["731f8608-ad5b-491e-a4d4-2bb0c423fed5"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Allegiant Health"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (69168-432-06)", "package_ndc": "69168-432-06", "marketing_start_date": "20231106"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (69168-432-07) / 10 TABLET in 1 BOTTLE", "package_ndc": "69168-432-07", "marketing_start_date": "20220518"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (69168-432-26) / 20 TABLET in 1 BOTTLE", "package_ndc": "69168-432-26", "marketing_start_date": "20220518"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (69168-432-30)", "package_ndc": "69168-432-30", "marketing_start_date": "20231106"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (69168-432-50)", "package_ndc": "69168-432-50", "marketing_start_date": "20220608"}, {"sample": false, "description": "200 TABLET in 1 BOTTLE (69168-432-98)", "package_ndc": "69168-432-98", "marketing_start_date": "20220518"}], "brand_name": "Mucus Relief DM Immediate Release", "product_id": "69168-432_751cf188-7b5f-4f9d-ba3e-8ce7997ecd31", "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": "69168-432", "generic_name": "Mucus Relief DM", "labeler_name": "Allegiant Health", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief DM", "brand_name_suffix": "Immediate Release", "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": "20220518", "listing_expiration_date": "20261231"}