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HAND SANITIZER
HAND SANITIZER - 51706-500-01 - (ALCOHOL)
Drug Information of HAND SANITIZER
| Product NDC: | 51706-500 |
| Proprietary Name: | HAND SANITIZER |
| Non Proprietary Name: | ALCOHOL |
| Active Ingredient(s): | 62 mL/100mL & nbsp; ALCOHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of HAND SANITIZER
| Product NDC: | 51706-500 |
| Labeler Name: | Landy International |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120614 |
Package Information of HAND SANITIZER
| Package NDC: | 51706-500-01 |
| Package Description: | 29 mL in 1 BOTTLE, PLASTIC (51706-500-01) |
NDC Information of HAND SANITIZER
| NDC Code | 51706-500-01 |
| Proprietary Name | HAND SANITIZER |
| Package Description | 29 mL in 1 BOTTLE, PLASTIC (51706-500-01) |
| Product NDC | 51706-500 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALCOHOL |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20120614 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Landy International |
| Substance Name | ALCOHOL |
| Strength Number | 62 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
