severe cold daytime
Generic: acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl
Labeler: cvs pharmacyDrug Facts
Product Profile
Brand Name
severe cold daytime
Generic Name
acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl
Labeler
cvs pharmacy
Dosage Form
CAPSULE
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
69842-505
Product ID
69842-505_16ba95c0-d108-4cd7-bb95-07cd8afc89b5
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Marketing Start
2019-12-27
Marketing End
2026-12-27
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69842505
Hyphenated Format
69842-505
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
severe cold daytime (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
- 16 BLISTER PACK in 1 CARTON (69842-505-16) / 1 CAPSULE 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": "16ba95c0-d108-4cd7-bb95-07cd8afc89b5", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0050428381885"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1656815"], "spl_set_id": ["258d27a9-fea6-4076-8dfa-77c7e982d250"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["CVS Pharmacy"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "16 BLISTER PACK in 1 CARTON (69842-505-16) / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "69842-505-16", "marketing_end_date": "20261227", "marketing_start_date": "20191227"}], "brand_name": "Severe Cold Daytime", "product_id": "69842-505_16ba95c0-d108-4cd7-bb95-07cd8afc89b5", "dosage_form": "CAPSULE", "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": "69842-505", "generic_name": "Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl", "labeler_name": "CVS Pharmacy", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Severe Cold", "brand_name_suffix": "Daytime", "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_end_date": "20261227", "marketing_start_date": "20191227"}