Product NDC: | 49035-109 |
Proprietary Name: | winter vanilla hand sanitizer |
Non Proprietary Name: | Alcohol |
Active Ingredient(s): | 75 1/100mL & nbsp; Alcohol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49035-109 |
Labeler Name: | Wal-Mart Stores Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333E |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130522 |
Package NDC: | 49035-109-02 |
Package Description: | 1 BOTTLE, PLASTIC in 1 PACKAGE (49035-109-02) > 30 mL in 1 BOTTLE, PLASTIC (49035-109-01) |
NDC Code | 49035-109-02 |
Proprietary Name | winter vanilla hand sanitizer |
Package Description | 1 BOTTLE, PLASTIC in 1 PACKAGE (49035-109-02) > 30 mL in 1 BOTTLE, PLASTIC (49035-109-01) |
Product NDC | 49035-109 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Alcohol |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20130522 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Wal-Mart Stores Inc |
Substance Name | ALCOHOL |
Strength Number | 75 |
Strength Unit | 1/100mL |
Pharmaceutical Classes |