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 |