mucus relief dm maximum strength

Generic: guaifenesin, dextromethorphan hbr

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

Drug Facts

Product Profile

Brand Name mucus relief dm maximum strength
Generic Name guaifenesin, dextromethorphan hbr
Labeler harris teeter, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

dextromethorphan hydrobromide 60 mg/1, guaifenesin 1200 mg/1

Manufacturer
Harris Teeter, LLC

Identifiers & Regulatory

Product NDC 69256-834
Product ID 69256-834_086eb0c7-25b6-4e12-affa-9a6ec3ef6e33
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA209692
Marketing Start 2021-05-28
Marketing End 2026-05-28

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 69256834
Hyphenated Format 69256-834

Supplemental Identifiers

RxCUI
1099074
UPC
0072036736116
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 maximum strength (source: ndc)
Generic Name guaifenesin, dextromethorphan hbr (source: ndc)
Application Number ANDA209692 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 60 mg/1
  • 1200 mg/1
source: ndc
Packaging
  • 14 BLISTER PACK in 1 CARTON (69256-834-14) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (2)

dextromethorphan hydrobromide (60 mg/1) guaifenesin (1200 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "086eb0c7-25b6-4e12-affa-9a6ec3ef6e33", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0072036736116"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1099074"], "spl_set_id": ["8a2fdfb2-f852-45a2-8ee3-c2d3e6038dfc"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Harris Teeter, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "14 BLISTER PACK in 1 CARTON (69256-834-14)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "69256-834-14", "marketing_end_date": "20260528", "marketing_start_date": "20210528"}], "brand_name": "Mucus Relief DM Maximum Strength", "product_id": "69256-834_086eb0c7-25b6-4e12-affa-9a6ec3ef6e33", "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": "69256-834", "generic_name": "Guaifenesin, Dextromethorphan HBr", "labeler_name": "Harris Teeter, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief DM", "brand_name_suffix": "Maximum Strength", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "60 mg/1"}, {"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA209692", "marketing_category": "ANDA", "marketing_end_date": "20260528", "marketing_start_date": "20210528"}