mucus relief dm max
Generic: dextromethorphan hbr, guaifenesin
Labeler: rite aid corporationDrug Facts
Product Profile
Brand Name
mucus relief dm max
Generic Name
dextromethorphan hbr, guaifenesin
Labeler
rite aid corporation
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
dextromethorphan hydrobromide 60 mg/1, guaifenesin 1200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
11822-1812
Product ID
11822-1812_f61c91ea-be88-4994-9c34-4a794093dfa2
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA207602
Listing Expiration
2026-12-31
Marketing Start
2023-03-13
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
118221812
Hyphenated Format
11822-1812
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 max (source: ndc)
Generic Name
dextromethorphan hbr, guaifenesin (source: ndc)
Application Number
ANDA207602 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 60 mg/1
- 1200 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (11822-1812-0) / 14 TABLET, EXTENDED RELEASE in 1 BOTTLE
- 2 BOTTLE in 1 CARTON (11822-1812-1) / 14 TABLET, EXTENDED RELEASE in 1 BOTTLE
- 3 BOTTLE in 1 CARTON (11822-1812-2) / 14 TABLET, EXTENDED RELEASE in 1 BOTTLE
Packages (3)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f61c91ea-be88-4994-9c34-4a794093dfa2", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1099074"], "spl_set_id": ["a5fd7378-fd7b-400b-a374-0f3bee37702d"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Rite Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (11822-1812-0) / 14 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "11822-1812-0", "marketing_start_date": "20230313"}, {"sample": false, "description": "2 BOTTLE in 1 CARTON (11822-1812-1) / 14 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "11822-1812-1", "marketing_start_date": "20230316"}, {"sample": false, "description": "3 BOTTLE in 1 CARTON (11822-1812-2) / 14 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "11822-1812-2", "marketing_start_date": "20230316"}], "brand_name": "mucus relief DM MAX", "product_id": "11822-1812_f61c91ea-be88-4994-9c34-4a794093dfa2", "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": "11822-1812", "generic_name": "dextromethorphan HBr, guaifenesin", "labeler_name": "Rite Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "mucus relief DM MAX", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "60 mg/1"}, {"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA207602", "marketing_category": "ANDA", "marketing_start_date": "20230313", "listing_expiration_date": "20261231"}