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Avant Foaming Hand Sanitizer
Avant Foaming Hand Sanitizer - 68306-109-01 - (Alcohol)
Drug Information of Avant Foaming Hand Sanitizer
| Product NDC: | 68306-109 |
| Proprietary Name: | Avant Foaming 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 Avant Foaming Hand Sanitizer
| Product NDC: | 68306-109 |
| Labeler Name: | B4 Ventures LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20101208 |
Package Information of Avant Foaming Hand Sanitizer
| Package NDC: | 68306-109-01 |
| Package Description: | 530 mL in 1 BOTTLE, PUMP (68306-109-01) |
NDC Information of Avant Foaming Hand Sanitizer
| NDC Code | 68306-109-01 |
| Proprietary Name | Avant Foaming Hand Sanitizer |
| Package Description | 530 mL in 1 BOTTLE, PUMP (68306-109-01) |
| Product NDC | 68306-109 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Alcohol |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20101208 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | B4 Ventures LLC |
| Substance Name | ALCOHOL |
| Strength Number | 62 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
