| Product NDC: | 51098-742 |
| Proprietary Name: | Hands First |
| Non Proprietary Name: | Benzalkonium Chloride, Allantoin |
| Active Ingredient(s): | 5; 1.3 g/1000mL; mL/1000mL & nbsp; Benzalkonium Chloride, Allantoin |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 51098-742 |
| Labeler Name: | Avadim II LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100801 |
| Package NDC: | 51098-742-02 |
| Package Description: | 360 mL in 1 BOTTLE, PLASTIC (51098-742-02) |
| NDC Code | 51098-742-02 |
| Proprietary Name | Hands First |
| Package Description | 360 mL in 1 BOTTLE, PLASTIC (51098-742-02) |
| Product NDC | 51098-742 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzalkonium Chloride, Allantoin |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100801 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Avadim II LLC |
| Substance Name | ALLANTOIN; BENZALKONIUM CHLORIDE |
| Strength Number | 5; 1.3 |
| Strength Unit | g/1000mL; mL/1000mL |
| Pharmaceutical Classes |