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Day Time - 63941-142-06 - (Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride)
Drug Information of Day Time
| Product NDC: | 63941-142 |
| Proprietary Name: | Day Time |
| Non Proprietary Name: | Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride |
| Active Ingredient(s): | 325; 10; 5 mg/15mL; mg/15mL; mg/15mL & nbsp; Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Day Time
| Product NDC: | 63941-142 |
| Labeler Name: | Best Choice |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090813 |
Package Information of Day Time
| Package NDC: | 63941-142-06 |
| Package Description: | 177 mL in 1 BOTTLE, PLASTIC (63941-142-06) |
NDC Information of Day Time
| NDC Code | 63941-142-06 |
| Proprietary Name | Day Time |
| Package Description | 177 mL in 1 BOTTLE, PLASTIC (63941-142-06) |
| Product NDC | 63941-142 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20090813 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Best Choice |
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 325; 10; 5 |
| Strength Unit | mg/15mL; mg/15mL; mg/15mL |
| Pharmaceutical Classes |
