Product NDC: | 37000-556 |
Proprietary Name: | Vicks Childrens NyQuil |
Non Proprietary Name: | Chlorpheniramine maleate and Dextromethorphan Hydrobromide |
Active Ingredient(s): | 2; 15 mg/15mL; mg/15mL & nbsp; Chlorpheniramine maleate and Dextromethorphan Hydrobromide |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 37000-556 |
Labeler Name: | The Procter & Gamble Manufacturing Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110622 |
Package NDC: | 37000-556-08 |
Package Description: | 236 mL in 1 BOTTLE, PLASTIC (37000-556-08) |
NDC Code | 37000-556-08 |
Proprietary Name | Vicks Childrens NyQuil |
Package Description | 236 mL in 1 BOTTLE, PLASTIC (37000-556-08) |
Product NDC | 37000-556 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Chlorpheniramine maleate and Dextromethorphan Hydrobromide |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20110622 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | The Procter & Gamble Manufacturing Company |
Substance Name | CHLORPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE |
Strength Number | 2; 15 |
Strength Unit | mg/15mL; mg/15mL |
Pharmaceutical Classes |