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Hand Sanitizer
Hand Sanitizer - 75887-001-03 - (ALCOHOL)
Drug Information of Hand Sanitizer
| Product NDC: | 75887-001 |
| Proprietary Name: | Hand Sanitizer |
| Non Proprietary Name: | ALCOHOL |
| Active Ingredient(s): | 5 mL/8mL & nbsp; ALCOHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hand Sanitizer
| Product NDC: | 75887-001 |
| Labeler Name: | Aztex Enterprises |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110118 |
Package Information of Hand Sanitizer
| Package NDC: | 75887-001-03 |
| Package Description: | 8 mL in 1 BOTTLE, SPRAY (75887-001-03) |
NDC Information of Hand Sanitizer
| NDC Code | 75887-001-03 |
| Proprietary Name | Hand Sanitizer |
| Package Description | 8 mL in 1 BOTTLE, SPRAY (75887-001-03) |
| Product NDC | 75887-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALCOHOL |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20110118 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Aztex Enterprises |
| Substance Name | ALCOHOL |
| Strength Number | 5 |
| Strength Unit | mL/8mL |
| Pharmaceutical Classes |
