vicks nyquil severe honey flavor cold and flu

Generic: acetaminophen, dextromethrophan, doxylamine succinate, phenylephrine hcl

Labeler: procter & gamble manufacturing company
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name vicks nyquil severe honey flavor cold and flu
Generic Name acetaminophen, dextromethrophan, doxylamine succinate, phenylephrine hcl
Labeler procter & gamble manufacturing company
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

acetaminophen 325 mg/15mL, dextromethorphan hydrobromide 10 mg/15mL, doxylamine succinate 6.25 mg/15mL, phenylephrine hydrochloride 5 mg/15mL

Manufacturer
Procter & Gamble Manufacturing Company

Identifiers & Regulatory

Product NDC 69423-807
Product ID 69423-807_4040f959-06a0-1b87-e063-6394a90a51ed
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2021-07-07

Pharmacologic Class

Classes
adrenergic alpha1-agonists [moa] antihistamine [epc] histamine receptor antagonists [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 69423807
Hyphenated Format 69423-807

Supplemental Identifiers

RxCUI
1431245
UPC
0323900041615
UNII
362O9ITL9D 9D2RTI9KYH V9BI9B5YI2 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 nyquil severe honey flavor cold and flu (source: ndc)
Generic Name acetaminophen, dextromethrophan, doxylamine succinate, phenylephrine hcl (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/15mL
  • 10 mg/15mL
  • 6.25 mg/15mL
  • 5 mg/15mL
source: ndc
Packaging
  • 236 mL in 1 BOTTLE, PLASTIC (69423-807-08)
  • 354 mL in 1 BOTTLE, PLASTIC (69423-807-12)
source: ndc

Packages (2)

Ingredients (4)

acetaminophen (325 mg/15mL) dextromethorphan hydrobromide (10 mg/15mL) doxylamine succinate (6.25 mg/15mL) phenylephrine hydrochloride (5 mg/15mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4040f959-06a0-1b87-e063-6394a90a51ed", "openfda": {"upc": ["0323900041615"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "V9BI9B5YI2", "04JA59TNSJ"], "rxcui": ["1431245"], "spl_set_id": ["04ca1e9c-f297-cbd6-e063-6294a90a3739"], "manufacturer_name": ["Procter & Gamble Manufacturing Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "236 mL in 1 BOTTLE, PLASTIC (69423-807-08)", "package_ndc": "69423-807-08", "marketing_start_date": "20210707"}, {"sample": false, "description": "354 mL in 1 BOTTLE, PLASTIC (69423-807-12)", "package_ndc": "69423-807-12", "marketing_start_date": "20210707"}], "brand_name": "VICKS NyQuil SEVERE HONEY FLAVOR COLD and FLU", "product_id": "69423-807_4040f959-06a0-1b87-e063-6394a90a51ed", "dosage_form": "LIQUID", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Antihistamine [EPC]", "Histamine Receptor Antagonists [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": "69423-807", "generic_name": "Acetaminophen, Dextromethrophan, Doxylamine succinate, Phenylephrine HCl", "labeler_name": "Procter & Gamble Manufacturing Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "VICKS NyQuil SEVERE HONEY FLAVOR", "brand_name_suffix": "COLD and FLU", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/15mL"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/15mL"}, {"name": "DOXYLAMINE SUCCINATE", "strength": "6.25 mg/15mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/15mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210707", "listing_expiration_date": "20261231"}