quality choice mucus relief dm dm

Generic: dextromethorphan hydrobromide / guaifenesin

Labeler: chain drug marketing association
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name quality choice mucus relief dm dm
Generic Name dextromethorphan hydrobromide / guaifenesin
Labeler chain drug marketing association
Dosage Form TABLET
Routes
ORAL
Active Ingredients

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

Manufacturer
Chain Drug Marketing Association

Identifiers & Regulatory

Product NDC 63868-753
Product ID 63868-753_07b36c8b-1869-45d2-90be-b40b0fdb4f65
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2012-08-01

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 63868753
Hyphenated Format 63868-753

Supplemental Identifiers

RxCUI
1147685
UPC
0635515955721
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 quality choice mucus relief dm dm (source: ndc)
Generic Name dextromethorphan hydrobromide / guaifenesin (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
  • 400 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (63868-753-50) / 50 TABLET in 1 BOTTLE
source: ndc

Packages (1)

63868-753-50 1 BOTTLE in 1 CARTON (63868-753-50) / 50 TABLET in 1 BOTTLE

Ingredients (2)

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

Linked Drug Pages (1)

Quality Choice Mucus Relief DM DM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "07b36c8b-1869-45d2-90be-b40b0fdb4f65", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0635515955721"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1147685"], "spl_set_id": ["1c33a01f-1186-4a19-b639-a9cd49245220"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Chain Drug Marketing Association"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (63868-753-50)  / 50 TABLET in 1 BOTTLE", "package_ndc": "63868-753-50", "marketing_start_date": "20120801"}], "brand_name": "Quality Choice Mucus Relief DM DM", "product_id": "63868-753_07b36c8b-1869-45d2-90be-b40b0fdb4f65", "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": "63868-753", "generic_name": "Dextromethorphan Hydrobromide / Guaifenesin", "labeler_name": "Chain Drug Marketing Association", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Quality Choice Mucus Relief DM", "brand_name_suffix": "DM", "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": "20120801", "listing_expiration_date": "20261231"}