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smart sense nighttime
smart sense nighttime - 49738-990-38 - (- acetaminophen, dextromethorphan hydrobromide and doxylamine succinate liquid)
Drug Information of smart sense nighttime
| Product NDC: | 49738-990 |
| Proprietary Name: | smart sense nighttime |
| Non Proprietary Name: | - acetaminophen, dextromethorphan hydrobromide and doxylamine succinate liquid |
| Active Ingredient(s): | 500; 15; 6.25 mg/15mL; mg/15mL; mg/15mL & nbsp; - acetaminophen, dextromethorphan hydrobromide and doxylamine succinate liquid |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of smart sense nighttime
| Product NDC: | 49738-990 |
| Labeler Name: | Kmart Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20101207 |
Package Information of smart sense nighttime
| Package NDC: | 49738-990-38 |
| Package Description: | 296 mL in 1 BOTTLE (49738-990-38) |
NDC Information of smart sense nighttime
| NDC Code | 49738-990-38 |
| Proprietary Name | smart sense nighttime |
| Package Description | 296 mL in 1 BOTTLE (49738-990-38) |
| Product NDC | 49738-990 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | - acetaminophen, dextromethorphan hydrobromide and doxylamine succinate liquid |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20101207 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Kmart Corporation |
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE |
| Strength Number | 500; 15; 6.25 |
| Strength Unit | mg/15mL; mg/15mL; mg/15mL |
| Pharmaceutical Classes |
