NDC 37000-699

Vicks Alcohol Free NyQuil Cold and Flu Nighttime Relief

Acetaminophen, Chlorpheniramine Maleate, And Dextromethorphan Hydrobromide

Vicks Alcohol Free NyQuil Cold and Flu Nighttime Relief is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by The Procter & Gamble Manufacturing Company. The primary component is Acetaminophen; Chlorpheniramine Maleate; Dextromethorphan Hydrobromide.

Product ID37000-699_3f505f4c-d92f-3819-e054-00144ff88e88
NDC37000-699
Product TypeHuman Otc Drug
Proprietary NameVicks Alcohol Free NyQuil Cold and Flu Nighttime Relief
Generic NameAcetaminophen, Chlorpheniramine Maleate, And Dextromethorphan Hydrobromide
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2010-06-01
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart341
Labeler NameThe Procter & Gamble Manufacturing Company
Substance NameACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE
Active Ingredient Strength325 mg/15mL; mg/15mL; mg/15mL
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 37000-699-12

354 mL in 1 BOTTLE, PLASTIC (37000-699-12)
Marketing Start Date2011-06-22
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 37000-699-06 [37000069906]

Vicks Alcohol Free NyQuil Cold and Flu Nighttime Relief LIQUID
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-06-01
Marketing End Date2015-03-01

NDC 37000-699-08 [37000069908]

Vicks Alcohol Free NyQuil Cold and Flu Nighttime Relief LIQUID
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-06-22
Marketing End Date2013-02-24

NDC 37000-699-10 [37000069910]

Vicks Alcohol Free NyQuil Cold and Flu Nighttime Relief LIQUID
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-06-01
Marketing End Date2015-03-01

NDC 37000-699-12 [37000069912]

Vicks Alcohol Free NyQuil Cold and Flu Nighttime Relief LIQUID
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Billing UnitML
Marketing Start Date2011-06-22

Drug Details

Active Ingredients

IngredientStrength
ACETAMINOPHEN325 mg/15mL

OpenFDA Data

SPL SET ID:0fe37f2e-cf13-451d-8988-e96a5712e359
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1046384
  • Medicade Reported Pricing

    37000069912 VICKS NYQUIL COLD & FLU LIQUID

    Pricing Unit: ML | Drug Type:

    NDC Crossover Matching brand name "Vicks Alcohol Free NyQuil Cold and Flu Nighttime Relief" or generic name "Acetaminophen, Chlorpheniramine Maleate, And Dextromethorphan Hydrobromide"

    NDCBrand NameGeneric Name
    50580-245Childrens TYLENOLAcetaminophen, Chlorpheniramine Maleate, and Dextromethorphan Hydrobromide
    11523-1305Coricidin HBP Maximum Strength FluAcetaminophen, Chlorpheniramine maleate, and Dextromethorphan Hydrobromide
    69842-792CVS ChildrensAcetaminophen, Chlorpheniramine Maleate, and Dextromethorphan Hydrobromide
    37000-450VicksAcetaminophen, Chlorpheniramine maleate, and Dextromethorphan Hydrobromide
    37000-768VicksAcetaminophen, Chlorpheniramine maleate, and Dextromethorphan Hydrobromide
    37000-699Vicks Alcohol Free NyQuilAcetaminophen, Chlorpheniramine maleate, and Dextromethorphan Hydrobromide
    37000-759Vicks ChildrensAcetaminophen, Chlorpheniramine maleate, and Dextromethorphan Hydrobromide
    69423-967Vicks DayQuil SevereAcetaminophen, Chlorpheniramine maleate, and Dextromethorphan Hydrobromide
    69423-899Vicks NyQuil Alcohol FreeAcetaminophen, Chlorpheniramine maleate, and Dextromethorphan Hydrobromide
    69423-968Vicks NyQuil SevereAcetaminophen, Chlorpheniramine maleate, and Dextromethorphan Hydrobromide
    37000-969Vicks SevereAcetaminophen, Chlorpheniramine maleate, and Dextromethorphan Hydrobromide
    37000-970Vicks SevereAcetaminophen, Chlorpheniramine maleate, and Dextromethorphan Hydrobromide

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.