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Vanilla Bean Antibacterial Hand Sanitizer
Vanilla Bean Antibacterial Hand Sanitizer - 75848-0900-0 - (ALCOHOL)
Drug Information of Vanilla Bean Antibacterial Hand Sanitizer
| Product NDC: | 75848-0900 |
| Proprietary Name: | Vanilla Bean Antibacterial Hand Sanitizer |
| Non Proprietary Name: | ALCOHOL |
| Active Ingredient(s): | 62 mL/100mL & nbsp; ALCOHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Vanilla Bean Antibacterial Hand Sanitizer
| Product NDC: | 75848-0900 |
| Labeler Name: | Harrison Specialty Co., Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120301 |
Package Information of Vanilla Bean Antibacterial Hand Sanitizer
| Package NDC: | 75848-0900-0 |
| Package Description: | 473 mL in 1 BOTTLE (75848-0900-0) |
NDC Information of Vanilla Bean Antibacterial Hand Sanitizer
| NDC Code | 75848-0900-0 |
| Proprietary Name | Vanilla Bean Antibacterial Hand Sanitizer |
| Package Description | 473 mL in 1 BOTTLE (75848-0900-0) |
| Product NDC | 75848-0900 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALCOHOL |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20120301 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Harrison Specialty Co., Inc. |
| Substance Name | ALCOHOL |
| Strength Number | 62 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
