mucus relief dm (70000-0491)

Drug Facts

Product Profile

Brand Name mucus relief dm

Generic Name guaifenesin, dextromethorphan hbr

Labeler cardinal health 110, llc. dba leader 70000

Dosage Form TABLET

Routes

ORAL

Active Ingredients

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

Manufacturer

CARDINAL HEALTH 110, LLC. DBA LEADER 70000

Identifiers & Regulatory

Product NDC 70000-0491

Product ID 70000-0491_29abc92c-70fa-4fed-8f4a-267174943ffe

Product Type HUMAN OTC DRUG

Marketing Category ANDA

Application Number ANDA209692

Marketing Start 2019-01-31

Marketing End 2026-08-28

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 700000491

Hyphenated Format 70000-0491

Supplemental Identifiers

RxCUI

1298324

UPC

0096295136890

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 (70000-0491-1) / 1 TABLET in 1 BLISTER PACK

source: ndc

Packages (1)

70000-0491-1 20 BLISTER PACK in 1 CARTON (70000-0491-1) / 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": "29abc92c-70fa-4fed-8f4a-267174943ffe", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0096295136890"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1298324"], "spl_set_id": ["e24fd894-5dee-4f46-aafa-fbf9f0b166fd"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["CARDINAL HEALTH 110, LLC. DBA LEADER 70000"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 BLISTER PACK in 1 CARTON (70000-0491-1)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "70000-0491-1", "marketing_end_date": "20260828", "marketing_start_date": "20190131"}], "brand_name": "Mucus Relief DM", "product_id": "70000-0491_29abc92c-70fa-4fed-8f4a-267174943ffe", "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": "70000-0491", "generic_name": "Guaifenesin, Dextromethorphan HBr", "labeler_name": "CARDINAL HEALTH 110, LLC. DBA LEADER 70000", "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": "20260828", "marketing_start_date": "20190131"}