ENVIROPURE- benzalkonium chloride liquid

EnviroPure by

Drug Labeling and Warnings

EnviroPure by is a Otc medication manufactured, distributed, or labeled by Cemi International, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antiseptic

Uses

 hand sanitizer to decrease bacteria on the skin

recommended for repeated use

for use when soap and water are not available

Warnings

Flammable, keep away from fire/flame

For external use only

Do not use

​ in children less than 2 months of age

on open skin wounds

When using this product do not get into eyes. In case of contact, rinse eyes thoroughly with water

Stop use and ask a doctor if

irritation and redness develop

condition persists for more than 72 hours

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

Directions

 wet hands thoroughly with product and allow to dry without wiping

supervise children under 6 years of age when using this product to avoid swallowing

Other information

store between 15-30°C (59-86°F)

avoid freezing and excessive heat above 40°C (104°F)

do not use if the cap is broken

INACTIVE INGREDIENT

Inactive ingredients urea, water

Questions? 973-575-6591

You may also report serious side effects to this phone number. Mon-Fri 9:00 AM- 5:00 PM

SPL UNCLASSIFIED SECTION

alcohol-free

triclosan-free & fragrance-free

BAC-D

BACTERIAL DEFENSE

©Copyright Windmill Health Products®
All Rights Reserved.

Distributed by: Windmill Health Products®
10 Henderson Drive
West Caldwell, NJ 07006

Made in the U.S.A.

WindmillVitamins.com

Packaging

INGREDIENTS AND APPEARANCE

ENVIROPURE 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73741-102
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
UREA (UNII: 8W8T17847W)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73741-102-28	3785 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/06/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/06/2020

Labeler - Cemi International, Inc (015038336)

Establishment
Name	Address	ID/FEI	Business Operations
Cemi International, Inc		015038336	manufacture(73741-102)