LATALIA SANITIZING WIPES- alcohol cloth

Latalia Sanitizing Wipes by

Drug Labeling and Warnings

Latalia Sanitizing Wipes by is a Otc medication manufactured, distributed, or labeled by INTERNATIONAL CONSUMER PRODUCTS (PVT) LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient[s]

Alcohol 80% v/v

Purpose

Antiseptic & Antibacterial

Use[s]

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only. Flammable.
Keep away from heat or flame

Do not use

• in children less than 2 months of age
• on open skin wounds

When using this product

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children.

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

Directions

• Wipe hands or all surfaces. Allow to dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

Store between 15-30C (59-86F)

• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

Glycerin, Hydrogen peroxide, Purified Water USP

Packge Labeling:20 wipes

Package Labeling:40 wipes

INGREDIENTS AND APPEARANCE

LATALIA SANITIZING WIPES 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80016-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.8 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80016-003-00	20 in 1 POUCH	10/01/2020
1		3.75 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
2	NDC: 80016-003-01	40 in 1 POUCH	03/01/2021
2		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 Drug	M003	10/01/2020

Labeler - INTERNATIONAL CONSUMER PRODUCTS (PVT) LTD (645811162)