tussin cough chest congestion
Generic: dextromethorphan hydrobromide, guaifenesin
Labeler: rite aid corporationDrug Facts
Product Profile
Brand Name
tussin cough chest congestion
Generic Name
dextromethorphan hydrobromide, guaifenesin
Labeler
rite aid corporation
Dosage Form
SOLUTION
Routes
Active Ingredients
dextromethorphan hydrobromide 20 mg/20mL, guaifenesin 400 mg/20mL
Manufacturer
Identifiers & Regulatory
Product NDC
11822-1332
Product ID
11822-1332_406f624c-add2-47d6-a895-fbdef9883388
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2023-03-02
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
118221332
Hyphenated Format
11822-1332
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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 cough chest congestion (source: ndc)
Generic Name
dextromethorphan hydrobromide, guaifenesin (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/20mL
- 400 mg/20mL
Packaging
- 1 BOTTLE in 1 CARTON (11822-1332-1) / 118 mL in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (11822-1332-2) / 237 mL in 1 BOTTLE
Packages (2)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "406f624c-add2-47d6-a895-fbdef9883388", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1020138"], "spl_set_id": ["86fc3723-5fc5-4de5-bd04-7774c2abe539"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Rite Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (11822-1332-1) / 118 mL in 1 BOTTLE", "package_ndc": "11822-1332-1", "marketing_start_date": "20230302"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11822-1332-2) / 237 mL in 1 BOTTLE", "package_ndc": "11822-1332-2", "marketing_start_date": "20230302"}], "brand_name": "tussin cough chest congestion", "product_id": "11822-1332_406f624c-add2-47d6-a895-fbdef9883388", "dosage_form": "SOLUTION", "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": "11822-1332", "generic_name": "Dextromethorphan Hydrobromide, Guaifenesin", "labeler_name": "Rite Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "tussin cough chest congestion", "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": "20230302", "listing_expiration_date": "20261231"}