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Night Time Original
Night Time Original - 70253-112-01 - (Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate)
Drug Information of Night Time Original
| Product NDC: | 70253-112 |
| Proprietary Name: | Night Time Original |
| Non Proprietary Name: | Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate |
| Active Ingredient(s): | 500; 15; 6.25 mg/15mL; mg/15mL; mg/15mL & nbsp; Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Night Time Original
| Product NDC: | 70253-112 |
| Labeler Name: | Nash-Finch Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20051108 |
Package Information of Night Time Original
| Package NDC: | 70253-112-01 |
| Package Description: | 296 mL in 1 BOTTLE, PLASTIC (70253-112-01) |
NDC Information of Night Time Original
| NDC Code | 70253-112-01 |
| Proprietary Name | Night Time Original |
| Package Description | 296 mL in 1 BOTTLE, PLASTIC (70253-112-01) |
| Product NDC | 70253-112 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20051108 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Nash-Finch Company |
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE |
| Strength Number | 500; 15; 6.25 |
| Strength Unit | mg/15mL; mg/15mL; mg/15mL |
| Pharmaceutical Classes |
