mucus relief dm max maximum strength

Generic: dextromethorphan hbr, guaifenesin

Labeler: quality choice (chain drug marketing association)
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief dm max maximum strength
Generic Name dextromethorphan hbr, guaifenesin
Labeler quality choice (chain drug marketing association)
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

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

Manufacturer
QUALITY CHOICE (Chain Drug Marketing Association)

Identifiers & Regulatory

Product NDC 63868-235
Product ID 63868-235_4f7077f9-5790-46dd-88dc-236cd702e250
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2016-03-31

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 63868235
Hyphenated Format 63868-235

Supplemental Identifiers

RxCUI
1020138
UPC
0635515953383
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 max maximum strength (source: ndc)
Generic Name dextromethorphan hbr, guaifenesin (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/20mL
  • 400 mg/20mL
source: ndc
Packaging
  • 177 mL in 1 BOTTLE, PLASTIC (63868-235-06)
source: ndc

Packages (1)

63868-235-06 177 mL in 1 BOTTLE, PLASTIC (63868-235-06)

Ingredients (2)

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

Linked Drug Pages (1)

Mucus Relief DM Max Maximum Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4f7077f9-5790-46dd-88dc-236cd702e250", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0635515953383"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1020138"], "spl_set_id": ["d56c80b9-1073-4bf6-bc4b-9d5e14c99f8e"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["QUALITY CHOICE (Chain Drug Marketing Association)"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "177 mL in 1 BOTTLE, PLASTIC (63868-235-06)", "package_ndc": "63868-235-06", "marketing_start_date": "20160331"}], "brand_name": "Mucus Relief DM Max Maximum Strength", "product_id": "63868-235_4f7077f9-5790-46dd-88dc-236cd702e250", "dosage_form": "LIQUID", "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": "63868-235", "generic_name": "Dextromethorphan HBr, Guaifenesin", "labeler_name": "QUALITY CHOICE (Chain Drug Marketing Association)", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief DM Max", "brand_name_suffix": "Maximum Strength", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/20mL"}, {"name": "GUAIFENESIN", "strength": "400 mg/20mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160331", "listing_expiration_date": "20261231"}