Laupro Antiseptic Hand Sanitizing Wipes

Laupro Antiseptic Hand Sanitizing Wipes by

Drug Labeling and Warnings

Laupro Antiseptic Hand Sanitizing Wipes by is a Otc medication manufactured, distributed, or labeled by ENTAID INTERNATIONAL CORPORATION JOINT STOCK COMPANY. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

LAUPRO ANTISEPTIC HAND SANITIZING WIPES- benzalkonium chloride cloth 
ENTAID INTERNATIONAL CORPORATION JOINT STOCK COMPANY

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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Laupro Antiseptic Hand Sanitizing Wipes

Drug Facts

Active ingredient

Benzalkonium chloride 0.13%

Purpose

Antiseptic

Use

For hand washing to decrease bacteria on the skin

Warnings

For external use only.

Do not use

in the eyes

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 Poison Control Center right away.

Directions

Wet hands thoroughly with product and allow to dry without wiping

Inactive ingredients

Water, Glycerin, Decyl Glucoside, Phenoxyethanol, Fragrance, Aloe Vera Leaf Extract, Ethanol.

Questions or Comments?

415-851-1914

Package Labeling:

LAUPRO ANTISEPTIC HAND SANITIZING WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80275-000
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
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80275-000-01	75 in 1 CANISTER	10/07/2020
1		4.4 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	10/07/2020

Labeler - ENTAID INTERNATIONAL CORPORATION JOINT STOCK COMPANY (673067577)

Revised: 10/2020

Document Id: b17b586a-02ab-0b1d-e053-2995a90ae7a6

34390-5

Set id: 5d9323d4-eea5-4bda-ae9f-2b9fa1d104ea

Version: 1

Effective Time: 20201012

 

ENTAID INTER