tussin

Generic: dextromethorphan hbr, guaifenesin

Labeler: h e b
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name tussin
Generic Name dextromethorphan hbr, guaifenesin
Labeler h e b
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

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

Manufacturer
H E B

Identifiers & Regulatory

Product NDC 37808-639
Product ID 37808-639_5ad97f47-bc42-4590-9c7a-f0cd28a24cc1
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2018-09-24

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 37808639
Hyphenated Format 37808-639

Supplemental Identifiers

RxCUI
1020138
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 (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
  • 1 BOTTLE in 1 CARTON (37808-639-26) / 118 mL in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (37808-639-34) / 237 mL in 1 BOTTLE
source: ndc

Packages (2)

37808-639-26 1 BOTTLE in 1 CARTON (37808-639-26) / 118 mL in 1 BOTTLE 37808-639-34 1 BOTTLE in 1 CARTON (37808-639-34) / 237 mL in 1 BOTTLE

Ingredients (2)

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

Linked Drug Pages (1)

tussin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5ad97f47-bc42-4590-9c7a-f0cd28a24cc1", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1020138"], "spl_set_id": ["7c24c59c-7549-4c64-95f8-4bf755cd6f61"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (37808-639-26)  / 118 mL in 1 BOTTLE", "package_ndc": "37808-639-26", "marketing_start_date": "20180925"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (37808-639-34)  / 237 mL in 1 BOTTLE", "package_ndc": "37808-639-34", "marketing_start_date": "20180924"}], "brand_name": "tussin", "product_id": "37808-639_5ad97f47-bc42-4590-9c7a-f0cd28a24cc1", "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": "37808-639", "generic_name": "Dextromethorphan HBr, Guaifenesin", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "tussin", "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": "20180924", "listing_expiration_date": "20261231"}