daytime cold and flu
Generic: acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl
Labeler: kroger companyDrug Facts
Product Profile
Brand Name
daytime cold and flu
Generic Name
acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl
Labeler
kroger company
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
acetaminophen 325 mg/1, dextromethorphan hydrobromide 10 mg/1, guaifenesin 200 mg/1, phenylephrine hydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
41226-675
Product ID
41226-675_35c8c6ce-c850-6d95-e063-6294a90afe26
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2025-05-26
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
41226675
Hyphenated Format
41226-675
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
daytime cold and flu (source: ndc)
Generic Name
acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 325 mg/1
- 10 mg/1
- 200 mg/1
- 5 mg/1
Packaging
- 2 BLISTER PACK in 1 CARTON (41226-675-24) / 12 TABLET, FILM COATED in 1 BLISTER PACK
Packages (1)
Ingredients (4)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "35c8c6ce-c850-6d95-e063-6294a90afe26", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1110988"], "spl_set_id": ["30d4a6c6-895e-3741-e063-6294a90ab192"], "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": "2 BLISTER PACK in 1 CARTON (41226-675-24) / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "41226-675-24", "marketing_start_date": "20250526"}], "brand_name": "Daytime Cold and Flu", "product_id": "41226-675_35c8c6ce-c850-6d95-e063-6294a90afe26", "dosage_form": "TABLET, FILM COATED", "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": "41226-675", "generic_name": "Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl", "labeler_name": "KROGER COMPANY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Daytime Cold and Flu", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/1"}, {"name": "GUAIFENESIN", "strength": "200 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250526", "listing_expiration_date": "20261231"}