day cold and flu
Generic: acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl
Labeler: target corporationDrug Facts
Product Profile
Brand Name
day cold and flu
Generic Name
acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl
Labeler
target corporation
Dosage Form
TABLET, 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
11673-347
Product ID
11673-347_2b941963-8a8d-4148-e063-6294a90a1dfb
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2025-04-01
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
11673347
Hyphenated Format
11673-347
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
day 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 (11673-347-02) / 10 TABLET, 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": "2b941963-8a8d-4148-e063-6294a90a1dfb", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1110988"], "spl_set_id": ["2b941963-8a8c-4148-e063-6294a90a1dfb"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["TARGET CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (11673-347-02) / 10 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "11673-347-02", "marketing_start_date": "20250401"}], "brand_name": "DAY COLD AND FLU", "product_id": "11673-347_2b941963-8a8d-4148-e063-6294a90a1dfb", "dosage_form": "TABLET, 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": "11673-347", "generic_name": "acetaminophen, dextromethorphan HBr, guaifenesin, phenylephrine HCl", "labeler_name": "TARGET CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DAY 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": "20250401", "listing_expiration_date": "20261231"}