vicks dayquil severe nyquil severe honey flavor cold and flu

Generic: acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl and doxylamine succinate

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

Drug Facts

Product Profile

Brand Name vicks dayquil severe nyquil severe honey flavor cold and flu
Generic Name acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl and doxylamine succinate
Labeler the procter & gamble manufacturing company
Dosage Form KIT
Routes
ORAL
Manufacturer
The Procter & Gamble Manufacturing Company

Identifiers & Regulatory

Product NDC 69423-808
Product ID 69423-808_4040ea46-01f2-3885-e063-6294a90ae98e
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2020-04-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69423808
Hyphenated Format 69423-808

Supplemental Identifiers

RxCUI
1369842 1431245 2637731

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 severe nyquil severe honey flavor cold and flu (source: ndc)
Generic Name acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl and doxylamine succinate (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 ml
  • 325 mg
  • 10 mg
  • 6.25 mg
  • 5 mg
  • 200 mg
source: label
Packaging
  • 1 KIT in 1 CARTON (69423-808-24) * 354 mL in 1 BOTTLE * 354 mL in 1 BOTTLE
source: ndc

Packages (1)

69423-808-24 1 KIT in 1 CARTON (69423-808-24) * 354 mL in 1 BOTTLE * 354 mL in 1 BOTTLE

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

VICKS DayQuil SEVERE NyQuil SEVERE HONEY FLAVOR COLD and FLU ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4040ea46-01f2-3885-e063-6294a90ae98e", "openfda": {"rxcui": ["1369842", "1431245", "2637731"], "spl_set_id": ["fd03769c-2fd6-1c22-e053-6394a90a12f6"], "manufacturer_name": ["The Procter & Gamble Manufacturing Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (69423-808-24)  *  354 mL in 1 BOTTLE *  354 mL in 1 BOTTLE", "package_ndc": "69423-808-24", "marketing_start_date": "20200428"}], "brand_name": "VICKS DayQuil SEVERE NyQuil SEVERE HONEY FLAVOR COLD and FLU", "product_id": "69423-808_4040ea46-01f2-3885-e063-6294a90ae98e", "dosage_form": "KIT", "product_ndc": "69423-808", "generic_name": "Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl and Doxylamine succinate", "labeler_name": "The Procter & Gamble Manufacturing Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "VICKS DayQuil SEVERE NyQuil SEVERE HONEY FLAVOR", "brand_name_suffix": "COLD and FLU", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200428", "listing_expiration_date": "20261231"}