mucus relief dm

Generic: guaifenesin and dextromethorphan hbr

Labeler: harris teeter
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief dm
Generic Name guaifenesin and dextromethorphan hbr
Labeler harris teeter
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

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

Manufacturer
Harris Teeter

Identifiers & Regulatory

Product NDC 72036-012
Product ID 72036-012_0d3ca637-f84d-4e85-aac3-94113a4ece11
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA206941
Listing Expiration 2026-12-31
Marketing Start 2024-08-16

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 72036012
Hyphenated Format 72036-012

Supplemental Identifiers

RxCUI
1298324
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 and dextromethorphan hbr (source: ndc)
Application Number ANDA206941 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
  • 600 mg/1
source: ndc
Packaging
  • 2 BLISTER PACK in 1 CARTON (72036-012-20) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (2)

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0d3ca637-f84d-4e85-aac3-94113a4ece11", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1298324"], "spl_set_id": ["17eee39b-5a7a-ba20-e063-6294a90ac392"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Harris Teeter"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (72036-012-20)  / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "72036-012-20", "marketing_start_date": "20240816"}], "brand_name": "MUCUS RELIEF DM", "product_id": "72036-012_0d3ca637-f84d-4e85-aac3-94113a4ece11", "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": "72036-012", "generic_name": "Guaifenesin and Dextromethorphan HBr", "labeler_name": "Harris Teeter", "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": "ANDA206941", "marketing_category": "ANDA", "marketing_start_date": "20240816", "listing_expiration_date": "20261231"}