Product NDC: | 58686-013 |
Proprietary Name: | Shunfa Anti-Bacteria Spra |
Non Proprietary Name: | Didecyldimethyl Ammonium,Triclosan, Borneol, Benzalkonium Bromide |
Active Ingredient(s): | 3; 4; 3; 3 mg/1000mg; mg/1000mg; mg/1000mg; mg/1000mg & nbsp; Didecyldimethyl Ammonium,Triclosan, Borneol, Benzalkonium Bromide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 58686-013 |
Labeler Name: | Chengdu Shunfa Disinfection and Washing Technology Co Ltd |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20051030 |
Package NDC: | 58686-013-01 |
Package Description: | 30 mg in 1 BOTTLE, SPRAY (58686-013-01) |
NDC Code | 58686-013-01 |
Proprietary Name | Shunfa Anti-Bacteria Spra |
Package Description | 30 mg in 1 BOTTLE, SPRAY (58686-013-01) |
Product NDC | 58686-013 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Didecyldimethyl Ammonium,Triclosan, Borneol, Benzalkonium Bromide |
Dosage Form Name | SPRAY |
Route Name | TOPICAL |
Start Marketing Date | 20051030 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Chengdu Shunfa Disinfection and Washing Technology Co Ltd |
Substance Name | BENZALKONIUM BROMIDE; BORNEOL; DIDECYLDIMETHYLAMMONIUM; TRICLOSAN |
Strength Number | 3; 4; 3; 3 |
Strength Unit | mg/1000mg; mg/1000mg; mg/1000mg; mg/1000mg |
Pharmaceutical Classes |