| Product NDC: | 11697-318 |
| Proprietary Name: | Forever Hand Sanitizer |
| Non Proprietary Name: | Alcohol |
| Active Ingredient(s): | 36.58 mL/59mL & nbsp; Alcohol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 11697-318 |
| Labeler Name: | Aloe Vera of America, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100816 |
| Package NDC: | 11697-318-02 |
| Package Description: | 59 mL in 1 BOTTLE, PLASTIC (11697-318-02) |
| NDC Code | 11697-318-02 |
| Proprietary Name | Forever Hand Sanitizer |
| Package Description | 59 mL in 1 BOTTLE, PLASTIC (11697-318-02) |
| Product NDC | 11697-318 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Alcohol |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20100816 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Aloe Vera of America, Inc. |
| Substance Name | ALCOHOL |
| Strength Number | 36.58 |
| Strength Unit | mL/59mL |
| Pharmaceutical Classes |