Home NDC 69423-899 Vicks NyQuil Alcohol Free
Product NDC 69423-899
11-digit product format 694230899
Labeler code 69423
Product ID 69423-899_5d18d9ea-6f08-6642-e063-6294a90a97a7
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen, Chlorpheniramine maleate, and Dextromethorphan Hydrobromide
Dosage form LIQUID
Route ORAL
Labeler The Procter & Gamble Manufacturing Company
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-01-20
Substance ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE
Active strength 650; 4; 30 mg/30mL; mg/30mL; mg/30mL
Pharmacologic classes Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Vicks NyQuil Alcohol Free
Brand name suffix Cold and Flu Nighttime Relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 650 mg/30mL CHLORPHENIRAMINE MALEATE 4 mg/30mL DEXTROMETHORPHAN HYDROBROMIDE 30 mg/30mL
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69423-899-12 Vicks NyQuil Alcohol FreeCold and Flu Nighttime Relief 354 mL in 1 BOTTLE, PLASTIC LIQUID 354 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69423-899 VICKS NYQUIL ALCOHOL FREE COLD AND FLU NIGHTTIME RELIEF (ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, AND DEXTROMETHORPHAN HYDROBROMIDE) LIQUID [THE PROCTER & GAMBLE MANUFACTURING COMPANY] 5 Current NDC, Legacy NDC, 1 package rows 20241012_ec57c15e-cb6d-44a9-e053-2a95a90ae774.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 98 of 180 · 3,583 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 69423-899-12 69423089912 354 mL in 1 BOTTLE, PLASTIC (69423-899-12) 354 ml 2021-01-20 0000-00-00 No No Current