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 – BUSINESS LOCATION 1. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

LAUPRO ANTISEPTIC HAND SANITIZING WIPES- alcohol cloth 
ENTAID INTERNATIONAL CORPORATION JOINT STOCK COMPANY – BUSINESS LOCATION 1

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

Ethyl Alcohol 75% (v/v)

Purpose

Antiseptic

Uses

• For hand washing to reduce bacteria on the skin.
• Recommended for repeated use

Warnings

Flammable. Keep away from fire or flame.

For external use only.

When using this product

do not use in or near the eyes. If contact occurs, rinse eyes thoroughly with water.

Stop using and ask a doctor if

irritation or rash appears and continues for more than 72 hours.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Center right away.

Directions

• Wet hands thoroughly with product and allow to dry
• Children under 6 years of age should be supervised when using Laupro

Inactive ingredient

Water

Other information

• Store in a well-ventilated and dry place below 104°F (40°C)
• Keep container tightly closed

Questions or Comments?

415-851-1914

Package Labeling:

LAUPRO ANTISEPTIC HAND SANITIZING WIPES 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80275-666
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.75 mL  in 1 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80275-666-88	75 in 1 CANISTER	11/12/2020
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	11/12/2020

Labeler - ENTAID INTERNATIONAL CORPORATION JOINT STOCK COMPANY – BUSINESS LOCATION 1 (673067577)

Revised: 11/2020

Document Id: b3ec09b9-7512-0895-e053-2a95a90a7840

34390-5

Set id: b3ec23ec-aec5-ed89-e053-2a95a90ae18b

Version: 1

Effective Time: 20201112

 

ENTAID INTERNATIONAL CORPORATION JOI