PROBLEND E3 FOAMING HAND SANITIZER- benzalkonium chloride soap

Problend E3 Foaming Hand Sanitizer by

Drug Labeling and Warnings

Problend E3 Foaming Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Seatex, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient Purpose

Benzalkonium Chloride 0.1%...................Antimicrobial

INDICATIONS & USAGE

Uses

For hand sanitizing to decrease bacteria on the skin.

Recommended for repeated use.

WHEN USING

When using this product Avoid contact with eyes. In case of eye contact, flush eyes with water. Do not ingest.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions

Pump a small amount of foam into palm of hand.

Rub thoroughly over all surffaces of both hands

Rub hands together briskly until dry.

INACTIVE INGREDIENT

Inactive Ingredients

Water, Cetrimonium Chloride, Laurtrimonium Chloride, Dihydroxyethyl Cocamine Oxide

STOP USE

Stop use and ask a doctor if irritation or redness develops and conditions persist.

PURPOSE

Antiseptic, Hand Sanitizer

WARNINGS

Warnings For External use only.

PRINCIPAL DISPLAY PANEL

3.785 L 76250-120-01

PRINCIPAL DISPLAY PANEL

1249 L 76250-120-30

PRINCIPAL DISPLAY PANEL

208 L 76250-120-55

PRINCIPAL DISPLAY PANEL

1041 L 76250-120-75

PRINCIPAL DISPLAY PANEL

1.25 L Front 76250-120-25

PRINCIPAL DISPLAY PANEL

1.25 L Back 76250-120-25

INGREDIENTS AND APPEARANCE

PROBLEND E3 FOAMING HAND SANITIZER 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76250-120
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)
DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76250-120-01	3785 g in 1 BOTTLE; Type 0: Not a Combination Product	11/13/2020
2	NDC: 76250-120-30	1249000 g in 1 TANK; Type 0: Not a Combination Product	11/13/2020
3	NDC: 76250-120-55	208000 g in 1 DRUM; Type 0: Not a Combination Product	11/13/2020
4	NDC: 76250-120-75	1041000 g in 1 TANK; Type 0: Not a Combination Product	11/13/2020
5	NDC: 76250-120-25	1250 g in 1 CARTRIDGE; Type 0: Not a Combination Product	08/20/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	11/13/2020

Labeler - Seatex, LLC (026647404)

Registrant - Seatex, LLC (026647404)

Establishment
Name	Address	ID/FEI	Business Operations
Seatex, LLC		026647404	label(76250-120) , manufacture(76250-120) , pack(76250-120)