mucus relief dm max

Generic: dextromethorphan hbr, guaifenesin

Labeler: rite aid corporation
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief dm max
Generic Name dextromethorphan hbr, guaifenesin
Labeler rite aid corporation
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

dextromethorphan hydrobromide 60 mg/1, guaifenesin 1200 mg/1

Manufacturer
Rite Aid Corporation

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)
expectorant [epc]
Physiologic Effect
decreased respiratory secretion viscosity [pe] increased respiratory secretions [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 118221812
Hyphenated Format 11822-1812

Supplemental Identifiers

RxCUI
1099074
UNII
9D2RTI9KYH 495W7451VQ
NUI
N0000193956 N0000008867 N0000009560

Packaging Origin

Original Packager
true

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 60 mg/1
  • 1200 mg/1
source: ndc
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
source: ndc

Packages (3)

Ingredients (2)

dextromethorphan hydrobromide (60 mg/1) guaifenesin (1200 mg/1)

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"}