Bortek E2 Foaming Hand Wash

Bortek E-2 Foaming Hand Wash by

Drug Labeling and Warnings

Bortek E-2 Foaming Hand Wash by is a Otc medication manufactured, distributed, or labeled by Bortek Industries. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

BORTEK E-2 FOAMING HAND WASH- benzalkonium chloride liquid 
Bortek Industries

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Bortek E2 Foaming Hand Wash

Drug Facts

Active ingredient

Benzalkonium chloride 0.13% w/w

Purpose

Antiseptic

Uses

Handwash to decrease bacteria on the skin that can potentially cause disease.

Warnings

For external use only.

When using this product keep away from eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor if irritation or redness develop or last more than 72 hours.

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

Directions

• Pump suffIcient amount of foam into palm of hand
• Rub foam thoroughly over all surfaces of both hands for 15 seconds, including the area under the fingernails
• Rinse with water and dry thoroughly.

Inactive ingredients

alcohol, cetrimonium chloride, chlorhexidine gluconate, cocamidopropyl PG-dimonium chloride phosphate, decyl glucoside, isopropyl alcohol, phenoxyethanol, polyquatemium 10, polyquatemium 11, water.

800-626-7835

BortekShop.com

Distributed by Bortek Industries, Inc., Mechanicsburg, PA 17055

Bortek® INDUSTRIES, INC.

E-2 ANTISEPTIC FOAMING HAND WASH

33.8 fl oz (1000 mL)

BORTEK E-2 FOAMING HAND WASH 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81731-401
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
ALCOHOL (UNII: 3K9958V90M)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYQUATERNIUM-10 (1000 MPA.S AT 2%) (UNII: GMR4PEN8PK)
POLYQUATERNIUM-11 (1000000 MW) (UNII: 0B44BS5IJS)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81731-401-01	1000 mL in 1 CONTAINER; Type 0: Not a Combination Product	04/12/2021	02/21/2022
2	NDC: 81731-401-11	1000 mL in 1 POUCH; Type 0: Not a Combination Product	02/21/2022	02/17/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/12/2021	02/17/2024

Labeler - Bortek Industries (014184014)

Revised: 1/2023

Document Id: f278ffa7-5098-06fc-e053-2995a90a6bb9

34390-5

Set id: bfcd86f2-17b2-a5a8-e053-2995a90ac1dd

Version: 3

Effective Time: 20230117