NDC 74680-111

Germ-Away

Antibacterial

Germ-Away is a Topical Cloth in the Human Otc Drug category. It is labeled and distributed by Unico International Trading Corp. The primary component is Benzalkonium Chloride.

Product ID74680-111_ada02f20-07f0-9e90-e053-2995a90a0e8b
NDC74680-111
Product TypeHuman Otc Drug
Proprietary NameGerm-Away
Generic NameAntibacterial
Dosage FormCloth
Route of AdministrationTOPICAL
Marketing Start Date2020-08-24
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333A
Labeler NameUnico International Trading Corp
Substance NameBENZALKONIUM CHLORIDE
Active Ingredient Strength0 1/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 74680-111-45

80 CLOTH in 1 CANISTER (74680-111-45)
Marketing Start Date2020-08-24
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Germ-Away" or generic name "Antibacterial"

NDCBrand NameGeneric Name
74680-102Germ-AwayAnti-microbial
74680-103Germ-AwayAnti-microbial
74680-104Germ-AwayAnti-microbial
74680-105Germ-AwayAnti-microbial
74680-106Germ-AwayAnti-microbial
74680-107Germ-AwayAnti-microbial
74680-108Germ-Awayantibacterial hand wipe
74680-110Germ-Awayanti-microbial
74680-111Germ-Awayantibacterial
74680-112Germ-AwayAnti-bacterial
76162-101AntibacterialAntibacterial
76162-102AntibacterialAntibacterial
76162-103AntibacterialAntibacterial
80751-300ANTIBACTERIALANTIBACTERIAL
78440-001NATURALANTIBACTERIAL
78440-002NATURAL SENSEANTIBACTERIAL

Trademark Results [Germ-Away]

Mark Image

Registration | Serial
Company
Trademark
Application Date
GERM-AWAY
GERM-AWAY
77897681 not registered Dead/Abandoned
Unico International Trading Corp.
2009-12-20
GERM-AWAY
GERM-AWAY
77142304 3523132 Dead/Cancelled
Unico International Trading Corp.
2007-03-28
GERM-AWAY
GERM-AWAY
73633464 not registered Dead/Abandoned
CASEY, IRENE
1986-12-03
GERM-AWAY
GERM-AWAY
73633464 not registered Dead/Abandoned
CASEY, LARRY J.
1986-12-03

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.