leader tussin cf
Generic: acetaminophen, dextromethorphan hydrobromide, guaifenesin
Labeler: cardinal health 110, llc. dba leaderDrug Facts
Product Profile
Brand Name
leader tussin cf
Generic Name
acetaminophen, dextromethorphan hydrobromide, guaifenesin
Labeler
cardinal health 110, llc. dba leader
Dosage Form
SOLUTION
Routes
Active Ingredients
acetaminophen 650 mg/20mL, dextromethorphan hydrobromide 20 mg/20mL, guaifenesin 400 mg/20mL
Manufacturer
Identifiers & Regulatory
Product NDC
70000-0739
Product ID
70000-0739_b8bbcafc-ef05-4fe1-b3bd-91f3d84f67aa
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2025-09-30
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
700000739
Hyphenated Format
70000-0739
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
leader tussin cf (source: ndc)
Generic Name
acetaminophen, dextromethorphan hydrobromide, guaifenesin (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 650 mg/20mL
- 20 mg/20mL
- 400 mg/20mL
Packaging
- 1 BOTTLE in 1 CARTON (70000-0739-1) / 118 mL in 1 BOTTLE
Packages (1)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b8bbcafc-ef05-4fe1-b3bd-91f3d84f67aa", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "495W7451VQ"], "rxcui": ["2680300"], "spl_set_id": ["f4ffe87b-0a62-44ac-b84a-08cf77cda7f5"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Cardinal Health 110, LLC. dba Leader"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (70000-0739-1) / 118 mL in 1 BOTTLE", "package_ndc": "70000-0739-1", "marketing_start_date": "20250930"}], "brand_name": "LEADER TUSSIN CF", "product_id": "70000-0739_b8bbcafc-ef05-4fe1-b3bd-91f3d84f67aa", "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": "70000-0739", "generic_name": "acetaminophen, dextromethorphan hydrobromide, guaifenesin", "labeler_name": "Cardinal Health 110, LLC. dba Leader", "product_type": "HUMAN OTC DRUG", "brand_name_base": "LEADER TUSSIN CF", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/20mL"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/20mL"}, {"name": "GUAIFENESIN", "strength": "400 mg/20mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250930", "listing_expiration_date": "20261231"}