mucus relief dm (11822-0733)

Drug Facts

Product Profile

Brand Name mucus relief dm

Generic Name guaifenesin, dextromethorphan hbr

Labeler rite aid corporation

Dosage Form TABLET

Routes

ORAL

Active Ingredients

dextromethorphan hydrobromide 30 mg/1, guaifenesin 600 mg/1

Manufacturer

Rite Aid Corporation

Identifiers & Regulatory

Product NDC 11822-0733

Product ID 11822-0733_6a9ea21a-5003-47b7-bac0-f7f218ce9b5d

Product Type HUMAN OTC DRUG

Marketing Category ANDA

Application Number ANDA209692

Marketing Start 2019-02-28

Marketing End 2026-12-28

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 118220733

Hyphenated Format 11822-0733

Supplemental Identifiers

RxCUI

1298324

UPC

0011822732994

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 (source: ndc)

Generic Name guaifenesin, dextromethorphan hbr (source: ndc)

Application Number ANDA209692 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

30 mg/1
600 mg/1

source: ndc

Packaging

20 BLISTER PACK in 1 CARTON (11822-0733-2) / 1 TABLET in 1 BLISTER PACK
40 BLISTER PACK in 1 CARTON (11822-0733-4) / 1 TABLET in 1 BLISTER PACK
68 BLISTER PACK in 1 CARTON (11822-0733-6) / 1 TABLET in 1 BLISTER PACK

source: ndc

Packages (3)

11822-0733-2 20 BLISTER PACK in 1 CARTON (11822-0733-2) / 1 TABLET in 1 BLISTER PACK 11822-0733-4 40 BLISTER PACK in 1 CARTON (11822-0733-4) / 1 TABLET in 1 BLISTER PACK 11822-0733-6 68 BLISTER PACK in 1 CARTON (11822-0733-6) / 1 TABLET in 1 BLISTER PACK

Ingredients (2)

dextromethorphan hydrobromide (30 mg/1) guaifenesin (600 mg/1)

Linked Drug Pages (1)

Mucus Relief DM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "6a9ea21a-5003-47b7-bac0-f7f218ce9b5d", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0011822732994"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1298324"], "spl_set_id": ["035693ed-d720-430b-98f5-fe4b5dec5db6"], "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": "20 BLISTER PACK in 1 CARTON (11822-0733-2)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "11822-0733-2", "marketing_end_date": "20261228", "marketing_start_date": "20190228"}, {"sample": false, "description": "40 BLISTER PACK in 1 CARTON (11822-0733-4)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "11822-0733-4", "marketing_end_date": "20261228", "marketing_start_date": "20190228"}, {"sample": false, "description": "68 BLISTER PACK in 1 CARTON (11822-0733-6)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "11822-0733-6", "marketing_end_date": "20261228", "marketing_start_date": "20190228"}], "brand_name": "Mucus Relief DM", "product_id": "11822-0733_6a9ea21a-5003-47b7-bac0-f7f218ce9b5d", "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": "11822-0733", "generic_name": "Guaifenesin, Dextromethorphan HBr", "labeler_name": "Rite Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief DM", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "30 mg/1"}, {"name": "GUAIFENESIN", "strength": "600 mg/1"}], "application_number": "ANDA209692", "marketing_category": "ANDA", "marketing_end_date": "20261228", "marketing_start_date": "20190228"}