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Shunfa Anti-Bacteria Spra - 58686-013-01 - (Didecyldimethyl Ammonium,Triclosan, Borneol, Benzalkonium Bromide)

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Drug Information of Shunfa Anti-Bacteria Spra

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)

Labeler Information of Shunfa Anti-Bacteria Spra

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 Information of Shunfa Anti-Bacteria Spra

Package NDC: 58686-013-01
Package Description: 30 mg in 1 BOTTLE, SPRAY (58686-013-01)

NDC Information of Shunfa Anti-Bacteria Spra

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

Complete Information of Shunfa Anti-Bacteria Spra


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