mucus relief dm immediate release

Generic: mucus relief dm

Labeler: allegiant health
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief dm immediate release
Generic Name mucus relief dm
Labeler allegiant health
Dosage Form TABLET
Routes
ORAL
Active Ingredients

dextromethorphan hydrobromide 20 mg/1, guaifenesin 400 mg/1

Manufacturer
Allegiant Health

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)
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 69168432
Hyphenated Format 69168-432

Supplemental Identifiers

RxCUI
1147685
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 immediate release (source: ndc)
Generic Name mucus relief dm (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
  • 400 mg/1
source: ndc
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)
source: ndc

Packages (6)

Ingredients (2)

dextromethorphan hydrobromide (20 mg/1) guaifenesin (400 mg/1)

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"}