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Antibacterial Wet Wipes - 50672-838-01 - (Benzalkonium Chloride)

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Drug Information of Antibacterial Wet Wipes

Product NDC: 50672-838
Proprietary Name: Antibacterial Wet Wipes
Non Proprietary Name: Benzalkonium Chloride
Active Ingredient(s): .1    g/100g & nbsp;   Benzalkonium Chloride
Administration Route(s): TOPICAL
Dosage Form(s): SWAB
Coding System: National Drug Codes(NDC)

Labeler Information of Antibacterial Wet Wipes

Product NDC: 50672-838
Labeler Name: MC Group Development Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20121112

Package Information of Antibacterial Wet Wipes

Package NDC: 50672-838-01
Package Description: 3.3 g in 1 POUCH (50672-838-01)

NDC Information of Antibacterial Wet Wipes

NDC Code 50672-838-01
Proprietary Name Antibacterial Wet Wipes
Package Description 3.3 g in 1 POUCH (50672-838-01)
Product NDC 50672-838
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Benzalkonium Chloride
Dosage Form Name SWAB
Route Name TOPICAL
Start Marketing Date 20121112
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name MC Group Development Ltd.
Substance Name BENZALKONIUM CHLORIDE
Strength Number .1
Strength Unit g/100g
Pharmaceutical Classes

Complete Information of Antibacterial Wet Wipes


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