Life Quality Sanitizer Wipes

Life Quality Sanitizer Wipes by

Drug Labeling and Warnings

Life Quality Sanitizer Wipes by is a Otc medication manufactured, distributed, or labeled by LABORATORIOS ESME S.A.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

LIFE QUALITY SANITIZER WIPES- benzalkonium chloride cloth 
LABORATORIOS ESME S.A.

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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Life Quality Sanitizer Wipes

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.1%

Purpose

Antibacterial

Uses

• for hand sanitizing to decrease bacteria on the skin.

Warnings

For external use only

When using this product

avoid contact ith eyes. In case of contact eye, flush with water.

Stop use and ask a doctor

if irritation or redness develops.

Keep out of reach of children.

Keep the packing closed in a dry and fresh place.

Throw away used wipes in trash. Do not flush.

Directions:

To open or close package, see illustrations. Remove wipe. Wipe hands thoroughly and allow to dry.

Inactive ingredients:

Non Woven Fabric, Aqua, Glycerin, Phenoxyethanol (and) Ethylhexylglycerin, Aloe Barbadensis Leaf Extract, Polysorbate 20, Fragrance, Tocopheryl Acetate, Triethanolamine.

Package Labeling:

LIFE QUALITY SANITIZER WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81349-002
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81349-002-01	40 in 1 POUCH	03/01/2021	01/31/2023
1		2.35 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/01/2021	01/31/2023

Labeler - LABORATORIOS ESME S.A. (970057626)

Revised: 11/2022

Document Id: ec830017-1430-6ae3-e053-2a95a90a81ee

34390-5

Set id: b8659866-cbc2-59c8-e053-2a95a90adaf6

Version: 2

Effective Time: 20221102