Product NDC: | 37000-699 |
Proprietary Name: | Vicks Alcohol Free NyQuil |
Non Proprietary Name: | Acetaminophen, Chlorpheniramine maleate, and Dextromethorphan Hydrobromide |
Active Ingredient(s): | 325; 2; 15 mg/15mL; mg/15mL; mg/15mL & nbsp; Acetaminophen, Chlorpheniramine maleate, and Dextromethorphan Hydrobromide |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 37000-699 |
Labeler Name: | Procter & Gamble Manufacturing Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100601 |
Package NDC: | 37000-699-08 |
Package Description: | 236 mL in 1 BOTTLE, PLASTIC (37000-699-08) |
NDC Code | 37000-699-08 |
Proprietary Name | Vicks Alcohol Free NyQuil |
Package Description | 236 mL in 1 BOTTLE, PLASTIC (37000-699-08) |
Product NDC | 37000-699 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Chlorpheniramine maleate, and Dextromethorphan Hydrobromide |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20100601 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Procter & Gamble Manufacturing Company |
Substance Name | ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE |
Strength Number | 325; 2; 15 |
Strength Unit | mg/15mL; mg/15mL; mg/15mL |
Pharmaceutical Classes |