NDC 50865-017

E2 SANITIZING HAND

E2 Sanitizing Hand

E2 SANITIZING HAND is a Topical Soap in the Human Otc Drug category. It is labeled and distributed by Kutol Products Company. The primary component is Benzalkonium Chloride.

Product ID50865-017_6533056f-1031-280b-e053-2991aa0a1178
NDC50865-017
Product TypeHuman Otc Drug
Proprietary NameE2 SANITIZING HAND
Generic NameE2 Sanitizing Hand
Dosage FormSoap
Route of AdministrationTOPICAL
Marketing Start Date2015-09-15
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333A
Labeler NameKUTOL PRODUCTS COMPANY
Substance NameBENZALKONIUM CHLORIDE
Active Ingredient Strength0 mg/mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 50865-017-03

209000 mL in 1 DRUM (50865-017-03)
Marketing Start Date2015-09-15
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50865-017-09 [50865001709]

E2 SANITIZING HAND SOAP
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-09-15

NDC 50865-017-07 [50865001707]

E2 SANITIZING HAND SOAP
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-09-15

NDC 50865-017-41 [50865001741]

E2 SANITIZING HAND SOAP
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-09-15

NDC 50865-017-67 [50865001767]

E2 SANITIZING HAND SOAP
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-09-15

NDC 50865-017-65 [50865001765]

E2 SANITIZING HAND SOAP
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-09-15

NDC 50865-017-03 [50865001703]

E2 SANITIZING HAND SOAP
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-09-15

Drug Details

Active Ingredients

IngredientStrength
BENZALKONIUM CHLORIDE.003 mg/mL

OpenFDA Data

SPL SET ID:70357eaf-8cd8-4c5e-b7a8-ae2fbba0ca2e
Manufacturer
UNII
UPC Code
  • 0686702017098
  • 0686702017074

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