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Vicks DayQuil
Vicks DayQuil - 37000-555-24 - (Acetaminophen, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride)
Drug Information of Vicks DayQuil
| Product NDC: | 37000-555 |
| Proprietary Name: | Vicks DayQuil |
| Non Proprietary Name: | Acetaminophen, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride |
| Active Ingredient(s): | 325; 10; 5 mg/15mL; mg/15mL; mg/15mL & nbsp; Acetaminophen, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Vicks DayQuil
| Product NDC: | 37000-555 |
| 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 Information of Vicks DayQuil
| Package NDC: | 37000-555-24 |
| Package Description: | 2 BOTTLE, PLASTIC in 1 PACKAGE, COMBINATION (37000-555-24) > 236 mL in 1 BOTTLE, PLASTIC |
NDC Information of Vicks DayQuil
| NDC Code | 37000-555-24 |
| Proprietary Name | Vicks DayQuil |
| Package Description | 2 BOTTLE, PLASTIC in 1 PACKAGE, COMBINATION (37000-555-24) > 236 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 37000-555 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride |
| 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 | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 325; 10; 5 |
| Strength Unit | mg/15mL; mg/15mL; mg/15mL |
| Pharmaceutical Classes |
