Product NDC: | 50260-200 |
Proprietary Name: | HAND SANITIZER |
Non Proprietary Name: | HAND SANITIZER |
Active Ingredient(s): | 62 mL/100mL & nbsp; HAND SANITIZER |
Administration Route(s): | PERCUTANEOUS |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50260-200 |
Labeler Name: | Fercy Personal Care Products Co Limited |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100201 |
Package NDC: | 50260-200-04 |
Package Description: | 20 mL in 1 BOTTLE, PLASTIC (50260-200-04) |
NDC Code | 50260-200-04 |
Proprietary Name | HAND SANITIZER |
Package Description | 20 mL in 1 BOTTLE, PLASTIC (50260-200-04) |
Product NDC | 50260-200 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | HAND SANITIZER |
Dosage Form Name | GEL |
Route Name | PERCUTANEOUS |
Start Marketing Date | 20100201 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Fercy Personal Care Products Co Limited |
Substance Name | ALCOHOL |
Strength Number | 62 |
Strength Unit | mL/100mL |
Pharmaceutical Classes |