tussin dm cough and chest congestion non drowsy

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 tussin dm cough and chest congestion non drowsy
Generic Name dextromethorphan hbr, guaifenesin
Labeler quality choice (chain drug marketing association)
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

dextromethorphan hydrobromide 20 mg/10mL, guaifenesin 200 mg/10mL

Manufacturer
QUALITY CHOICE (Chain Drug Marketing Association)

Identifiers & Regulatory

Product NDC 63868-868
Product ID 63868-868_c4509471-5b5e-4df1-991f-4de8dffd4d46
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2014-09-30

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 63868868
Hyphenated Format 63868-868

Supplemental Identifiers

RxCUI
996520
UPC
0635515981331
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 tussin dm cough and chest congestion non drowsy (source: ndc)
Generic Name dextromethorphan hbr, guaifenesin (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/10mL
  • 200 mg/10mL
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 BOX (63868-868-54) / 118 mL in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 BOX (63868-868-56) / 237 mL in 1 BOTTLE, PLASTIC
source: ndc

Packages (2)

63868-868-54 1 BOTTLE, PLASTIC in 1 BOX (63868-868-54) / 118 mL in 1 BOTTLE, PLASTIC 63868-868-56 1 BOTTLE, PLASTIC in 1 BOX (63868-868-56) / 237 mL in 1 BOTTLE, PLASTIC

Ingredients (2)

dextromethorphan hydrobromide (20 mg/10mL) guaifenesin (200 mg/10mL)

Linked Drug Pages (1)

Tussin DM Cough and Chest Congestion Non Drowsy ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c4509471-5b5e-4df1-991f-4de8dffd4d46", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0635515981331"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["996520"], "spl_set_id": ["5da9be32-9075-4eca-bb13-ce16330e39fa"], "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": "1 BOTTLE, PLASTIC in 1 BOX (63868-868-54)  / 118 mL in 1 BOTTLE, PLASTIC", "package_ndc": "63868-868-54", "marketing_start_date": "20140930"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (63868-868-56)  / 237 mL in 1 BOTTLE, PLASTIC", "package_ndc": "63868-868-56", "marketing_start_date": "20140930"}], "brand_name": "Tussin DM Cough and Chest Congestion Non Drowsy", "product_id": "63868-868_c4509471-5b5e-4df1-991f-4de8dffd4d46", "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": "63868-868", "generic_name": "Dextromethorphan HBr, Guaifenesin", "labeler_name": "QUALITY CHOICE (Chain Drug Marketing Association)", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Tussin DM Cough and Chest Congestion", "brand_name_suffix": "Non Drowsy", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/10mL"}, {"name": "GUAIFENESIN", "strength": "200 mg/10mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20140930", "listing_expiration_date": "20261231"}