Product NDC: | 50519-738 |
Proprietary Name: | Sani Spritz |
Non Proprietary Name: | ALCOHOL |
Active Ingredient(s): | .7 mL/mL & nbsp; ALCOHOL |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50519-738 |
Labeler Name: | American Industrial Supply, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20091231 |
Package NDC: | 50519-738-18 |
Package Description: | 50 mL in 1 BOTTLE, PLASTIC (50519-738-18) |
NDC Code | 50519-738-18 |
Proprietary Name | Sani Spritz |
Package Description | 50 mL in 1 BOTTLE, PLASTIC (50519-738-18) |
Product NDC | 50519-738 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ALCOHOL |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20091231 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | American Industrial Supply, Inc. |
Substance Name | ALCOHOL |
Strength Number | .7 |
Strength Unit | mL/mL |
Pharmaceutical Classes |