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SMART SENSE
SMART SENSE - 49738-478-32 - (ETHYL ALCOHOL)
Drug Information of SMART SENSE
| Product NDC: | 49738-478 |
| Proprietary Name: | SMART SENSE |
| Non Proprietary Name: | ETHYL ALCOHOL |
| Active Ingredient(s): | 700 mg/mL & nbsp; ETHYL ALCOHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SMART SENSE
| Product NDC: | 49738-478 |
| Labeler Name: | KMART CORPORATION |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130708 |
Package Information of SMART SENSE
| Package NDC: | 49738-478-32 |
| Package Description: | 946 mL in 1 BOTTLE, PLASTIC (49738-478-32) |
NDC Information of SMART SENSE
| NDC Code | 49738-478-32 |
| Proprietary Name | SMART SENSE |
| Package Description | 946 mL in 1 BOTTLE, PLASTIC (49738-478-32) |
| Product NDC | 49738-478 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ETHYL ALCOHOL |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20130708 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | KMART CORPORATION |
| Substance Name | ALCOHOL |
| Strength Number | 700 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
