mucus relief xpect

Generic: guaifensin, dextromethorphan

Labeler: midway importing inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief xpect
Generic Name guaifensin, dextromethorphan
Labeler midway importing inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

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

Manufacturer
Midway Importing Inc.

Identifiers & Regulatory

Product NDC 76095-012
Product ID 76095-012_24b26929-2f23-e5e7-e063-6394a90af59a
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2021-05-17

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 76095012
Hyphenated Format 76095-012

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 xpect (source: ndc)
Generic Name guaifensin, dextromethorphan (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
  • 400 mg/1
source: ndc
Packaging
  • 2 BLISTER PACK in 1 CARTON (76095-012-20) / 10 TABLET in 1 BLISTER PACK
  • 3 BLISTER PACK in 1 CARTON (76095-012-30) / 10 TABLET in 1 BLISTER PACK
source: ndc

Packages (2)

76095-012-20 2 BLISTER PACK in 1 CARTON (76095-012-20) / 10 TABLET in 1 BLISTER PACK 76095-012-30 3 BLISTER PACK in 1 CARTON (76095-012-30) / 10 TABLET in 1 BLISTER PACK

Ingredients (2)

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

Linked Drug Pages (1)

Mucus Relief Xpect ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "24b26929-2f23-e5e7-e063-6394a90af59a", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1147685"], "spl_set_id": ["c2c8bd26-bbf1-c2e6-e053-2995a90a86a7"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Midway Importing Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (76095-012-20)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "76095-012-20", "marketing_start_date": "20210519"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (76095-012-30)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "76095-012-30", "marketing_start_date": "20210519"}], "brand_name": "Mucus Relief Xpect", "product_id": "76095-012_24b26929-2f23-e5e7-e063-6394a90af59a", "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": "76095-012", "generic_name": "Guaifensin, Dextromethorphan", "labeler_name": "Midway Importing Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief Xpect", "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": "20210517", "listing_expiration_date": "20261231"}