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Vicks NyQuil
Vicks NyQuil - 37000-808-08 - (Acetaminophen, Dextromethorphan Hydrobromide, and Doxylamine succinate)
Drug Information of Vicks NyQuil
| Product NDC: | 37000-808 |
| Proprietary Name: | Vicks NyQuil |
| Non Proprietary Name: | Acetaminophen, Dextromethorphan Hydrobromide, and Doxylamine succinate |
| Active Ingredient(s): | 650; 30; 12.5 mg/30mL; mg/30mL; mg/30mL & nbsp; Acetaminophen, Dextromethorphan Hydrobromide, and Doxylamine succinate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Vicks NyQuil
| Product NDC: | 37000-808 |
| 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 Information of Vicks NyQuil
| Package NDC: | 37000-808-08 |
| Package Description: | 236 mL in 1 BOTTLE, PLASTIC (37000-808-08) |
NDC Information of Vicks NyQuil
| NDC Code | 37000-808-08 |
| Proprietary Name | Vicks NyQuil |
| Package Description | 236 mL in 1 BOTTLE, PLASTIC (37000-808-08) |
| Product NDC | 37000-808 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Dextromethorphan Hydrobromide, and Doxylamine succinate |
| 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; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE |
| Strength Number | 650; 30; 12.5 |
| Strength Unit | mg/30mL; mg/30mL; mg/30mL |
| Pharmaceutical Classes |
