Product NDC: | 62257-738 |
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: | 62257-738 |
Labeler Name: | ABC Compounding Co., Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20091031 |
Package NDC: | 62257-738-16 |
Package Description: | 236 mL in 1 BOTTLE, PLASTIC (62257-738-16) |
NDC Code | 62257-738-16 |
Proprietary Name | Sani-Spritz |
Package Description | 236 mL in 1 BOTTLE, PLASTIC (62257-738-16) |
Product NDC | 62257-738 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ALCOHOL |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20091031 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | ABC Compounding Co., Inc. |
Substance Name | ALCOHOL |
Strength Number | .7 |
Strength Unit | mL/mL |
Pharmaceutical Classes |