LOLA Hand Sanitizer by Alyk, Inc.

LOLA Hand Sanitizer by

Drug Labeling and Warnings

LOLA Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Alyk, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

LOLA HAND SANITIZER- alcohol spray 
Alyk, Inc.

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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Active Ingredient(s)

Ethyl Alcohol 67.0% v/v

Purpose

Antiseptic

Use

• For hand sanitizing to decrease bacteria on skin
• Recommended for repeated use

Warnings

• For external use only
• Flammable, keep away from fire or flame

Do not use

• Do not use internally
• Do not use on eyes

When using this product avoid contact with eyes. If in eyes, flush thoroughly with water.

Discontinue use and contact a doctor if irritation and redness develop and conditions persist for more than 72 hours.

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

Directions

• Place enough product in your palm to thoroughly cover your hands
• Rub hands together until dry
• Children under 6 years old should be supervised when using this product

Other information

• Use according to package label instructions
• Store in cool, well-ventilated place
• Avoid freezing or excessive heat

Inactive ingredients

Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Water

Package Label - Principal Display Panel

LOLA HAND SANITIZER 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81032-411
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	67 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81032-411-42	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	12/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	12/01/2020	10/31/2022

Labeler - Alyk, Inc. (079830975)

Revised: 1/2023

Document Id: f1ec09dd-1665-54f4-e053-2995a90ae66a

34390-5

Set id: b4026fcb-766d-5955-e053-2995a90ab926

Version: 2

Effective Time: 20230110

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