vicks dayquil and vicks nyquil severe cold and flu

Generic: acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 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 and vicks nyquil severe cold and flu
Generic Name acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, and doxylamine succinate
Labeler the procter & gamble manufacturing company
Dosage Form KIT
Manufacturer
The Procter & Gamble Manufacturing Company

Identifiers & Regulatory

Product NDC 37000-814
Product ID 37000-814_386574ec-d591-7230-e063-6394a90a99bb
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2013-07-22

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37000814
Hyphenated Format 37000-814

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 and vicks nyquil severe cold and flu (source: ndc)
Generic Name acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, and doxylamine succinate (source: ndc)
Application Number M012 (source: ndc)

Resolved Composition

Strengths
  • 15 ml
  • 325 mg
  • 10 mg
  • 200 mg
  • 5 mg
  • 30 ml
  • 650 mg
  • 20 mg
  • 12.5 mg
source: label
Packaging
  • 1 KIT in 1 PACKAGE (37000-814-24) * 354 mL in 1 BOTTLE, PLASTIC (37000-810-12) * 354 mL in 1 BOTTLE, PLASTIC (37000-812-12)
source: ndc

Packages (1)

37000-814-24 1 KIT in 1 PACKAGE (37000-814-24) * 354 mL in 1 BOTTLE, PLASTIC (37000-810-12) * 354 mL in 1 BOTTLE, PLASTIC (37000-812-12)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Vicks DayQuil and Vicks NyQuil Severe Cold and Flu ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "386574ec-d591-7230-e063-6394a90a99bb", "openfda": {"rxcui": ["1369842", "1431245", "2637731"], "spl_set_id": ["a17d0de4-85d1-47b7-ba72-3672ea65b397"], "manufacturer_name": ["The Procter & Gamble Manufacturing Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 PACKAGE (37000-814-24)  *  354 mL in 1 BOTTLE, PLASTIC (37000-810-12)  *  354 mL in 1 BOTTLE, PLASTIC (37000-812-12)", "package_ndc": "37000-814-24", "marketing_start_date": "20130722"}], "brand_name": "Vicks DayQuil and Vicks NyQuil Severe Cold and Flu", "product_id": "37000-814_386574ec-d591-7230-e063-6394a90a99bb", "dosage_form": "KIT", "product_ndc": "37000-814", "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, and doxylamine succinate", "labeler_name": "The Procter & Gamble Manufacturing Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Vicks DayQuil and Vicks NyQuil", "brand_name_suffix": "Severe Cold and Flu", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20130722", "listing_expiration_date": "20261231"}