vicks dayquil and vicks nyquil cold and flu

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

Identifiers & Regulatory

Product NDC 37000-033
Product ID 37000-033_4b447cb6-3afd-f7e9-e063-6394a90ae99a
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2027-12-31
Marketing Start 2013-08-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37000033
Hyphenated Format 37000-033

Supplemental Identifiers

RxCUI
1043400 1113705 2637726

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 cold and flu (source: ndc)
Generic Name acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride, and doxylamine succinate (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 ml
  • 650 mg
  • 30 mg
  • 12.5 mg
  • 15 ml
  • 325 mg
  • 10 mg
  • 5 mg
source: label
Packaging
  • 1 KIT in 1 PACKAGE (37000-033-24) * 354 mL in 1 BOTTLE, PLASTIC (69423-788-12) * 354 mL in 1 BOTTLE, PLASTIC (69423-789-12)
source: ndc

Packages (1)

37000-033-24 1 KIT in 1 PACKAGE (37000-033-24) * 354 mL in 1 BOTTLE, PLASTIC (69423-788-12) * 354 mL in 1 BOTTLE, PLASTIC (69423-789-12)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

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

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4b447cb6-3afd-f7e9-e063-6394a90ae99a", "openfda": {"rxcui": ["1043400", "1113705", "2637726"], "spl_set_id": ["416c6674-e4aa-6375-e054-00144ff8d46c"], "manufacturer_name": ["The Procter & Gamble Manufacturing Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 PACKAGE (37000-033-24)  *  354 mL in 1 BOTTLE, PLASTIC (69423-788-12)  *  354 mL in 1 BOTTLE, PLASTIC (69423-789-12)", "package_ndc": "37000-033-24", "marketing_start_date": "20130801"}], "brand_name": "Vicks DayQuil and Vicks NyQuil Cold and Flu", "product_id": "37000-033_4b447cb6-3afd-f7e9-e063-6394a90ae99a", "dosage_form": "KIT", "product_ndc": "37000-033", "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide, 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": "Cold and Flu", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20130801", "listing_expiration_date": "20271231"}