vicks dayquil hot remedy rapid relief multi-symptom cold and flu plus congestion

Generic: acetaminophen, dextromethorphan hbr, phenylephrine hcl

Labeler: procter & gamble manufactura s de rl de cv
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name vicks dayquil hot remedy rapid relief multi-symptom cold and flu plus congestion
Generic Name acetaminophen, dextromethorphan hbr, phenylephrine hcl
Labeler procter & gamble manufactura s de rl de cv
Dosage Form POWDER, FOR SOLUTION
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/5g, dextromethorphan hydrobromide 20 mg/5g, phenylephrine hydrochloride 10 mg/5g

Manufacturer
Procter & Gamble Manufactura S de RL de CV

Identifiers & Regulatory

Product NDC 58933-550
Product ID 58933-550_48824b85-d831-1ada-e063-6294a90a3793
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Marketing Start 2023-03-22
Marketing End 2027-06-30

Pharmacologic Class

Classes
adrenergic alpha1-agonists [moa] 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]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 58933550
Hyphenated Format 58933-550

Supplemental Identifiers

RxCUI
1189316
UNII
362O9ITL9D 9D2RTI9KYH 04JA59TNSJ

Packaging Origin

Original Packager
true

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 vicks dayquil hot remedy rapid relief multi-symptom cold and flu plus congestion (source: ndc)
Generic Name acetaminophen, dextromethorphan hbr, phenylephrine hcl (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/5g
  • 20 mg/5g
  • 10 mg/5g
source: ndc
Packaging
  • 5 g in 1 PACKET (58933-550-01)
  • 8 PACKET in 1 PACKAGE (58933-550-08) / 5 g in 1 PACKET
source: ndc

Packages (2)

Ingredients (3)

acetaminophen (500 mg/5g) dextromethorphan hydrobromide (20 mg/5g) phenylephrine hydrochloride (10 mg/5g)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48824b85-d831-1ada-e063-6294a90a3793", "openfda": {"unii": ["362O9ITL9D", "9D2RTI9KYH", "04JA59TNSJ"], "rxcui": ["1189316"], "spl_set_id": ["f77226c0-b6d5-9fd0-e053-6294a90a4b57"], "manufacturer_name": ["Procter & Gamble Manufactura S de RL de CV"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 g in 1 PACKET (58933-550-01)", "package_ndc": "58933-550-01", "marketing_end_date": "20270630", "marketing_start_date": "20230322"}, {"sample": false, "description": "8 PACKET in 1 PACKAGE (58933-550-08)  / 5 g in 1 PACKET", "package_ndc": "58933-550-08", "marketing_end_date": "20270630", "marketing_start_date": "20230322"}], "brand_name": "Vicks DayQuil HOT REMEDY RAPID RELIEF MULTI-SYMPTOM Cold and Flu plus Congestion", "product_id": "58933-550_48824b85-d831-1ada-e063-6294a90a3793", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "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": "58933-550", "generic_name": "Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl", "labeler_name": "Procter & Gamble Manufactura S de RL de CV", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Vicks DayQuil HOT REMEDY RAPID RELIEF MULTI-SYMPTOM", "brand_name_suffix": "Cold and Flu plus Congestion", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/5g"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/5g"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/5g"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20270630", "marketing_start_date": "20230322"}