severe cold and flu daytime
Generic: acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl
Labeler: kroger companyDrug Facts
Product Profile
Brand Name
severe cold and flu daytime
Generic Name
acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl
Labeler
kroger company
Dosage Form
LIQUID
Routes
Active Ingredients
acetaminophen 650 mg/30mL, dextromethorphan hydrobromide 20 mg/30mL, guaifenesin 400 mg/30mL, phenylephrine hydrochloride 10 mg/30mL
Manufacturer
Identifiers & Regulatory
Product NDC
41226-780
Product ID
41226-780_167122ff-90c5-7e8b-e063-6394a90a7b8a
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2024-04-30
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
41226780
Hyphenated Format
41226-780
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
severe cold and flu daytime (source: ndc)
Generic Name
acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 650 mg/30mL
- 20 mg/30mL
- 400 mg/30mL
- 10 mg/30mL
Packaging
- 354 mL in 1 BOTTLE (41226-780-01)
Packages (1)
Ingredients (4)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "167122ff-90c5-7e8b-e063-6394a90a7b8a", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1369842"], "spl_set_id": ["10106c90-f2f0-508e-e063-6294a90a544b"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["KROGER COMPANY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "354 mL in 1 BOTTLE (41226-780-01)", "package_ndc": "41226-780-01", "marketing_start_date": "20240430"}], "brand_name": "Severe Cold and Flu Daytime", "product_id": "41226-780_167122ff-90c5-7e8b-e063-6394a90a7b8a", "dosage_form": "LIQUID", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "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]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "41226-780", "generic_name": "Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl", "labeler_name": "KROGER COMPANY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Severe Cold and Flu Daytime", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/30mL"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/30mL"}, {"name": "GUAIFENESIN", "strength": "400 mg/30mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/30mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240430", "listing_expiration_date": "20261231"}