daytime cold and flu relief
Generic: acetaminohpen, dextromethorphan hbr, guaifenesin phenylephrine hcl
Labeler: walgreens co.Drug Facts
Product Profile
Brand Name
daytime cold and flu relief
Generic Name
acetaminohpen, dextromethorphan hbr, guaifenesin phenylephrine hcl
Labeler
walgreens co.
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
0363-7270
Product ID
0363-7270_447c5b5e-881c-994e-e063-6394a90a8752
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2021-02-02
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
03637270
Hyphenated Format
0363-7270
Supplemental Identifiers
RxCUI
UPC
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 relief (source: ndc)
Generic Name
acetaminohpen, 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, PLASTIC (0363-7270-12)
Packages (1)
Ingredients (4)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "447c5b5e-881c-994e-e063-6394a90a8752", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0311917031286"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1369842"], "spl_set_id": ["bfc58cd5-9815-43af-895d-ec6cbd10937e"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["WALGREENS CO."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "354 mL in 1 BOTTLE, PLASTIC (0363-7270-12)", "package_ndc": "0363-7270-12", "marketing_start_date": "20210202"}], "brand_name": "Daytime Cold and Flu Relief", "product_id": "0363-7270_447c5b5e-881c-994e-e063-6394a90a8752", "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": "0363-7270", "generic_name": "ACETAMINOHPEN, DEXTROMETHORPHAN HBr, GUAIFENESIN PHENYLEPHRINE HCL", "labeler_name": "WALGREENS CO.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Daytime Cold and Flu Relief", "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": "20210202", "listing_expiration_date": "20261231"}