Lysol ® Hand Sanitizer

Lysol by

Drug Labeling and Warnings

Lysol by is a Otc medication manufactured, distributed, or labeled by Reckitt Benckiser LLC, Precise Packaging LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

LYSOL HAND SANITIZER- alcohol solution 
Reckitt Benckiser LLC

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Lysol ®

Hand Sanitizer

Drug Facts

Active Ingredient

Ethyl alcohol 70% v/v

Purpose

Antimicrobial

Use

• Hand sanitizer to help reduce bacteria on the skin that could cause disease.
• Recommended for repeated use.

Warnings

Keep out of reach of children.

Flammable. Keep away from fire or flame.

For external use only,do not ingest. If swallowed, get medical help or contact a Poison Control Center right away.

When using this productdo not use in or near the eyes. In case of contact, rinse the eyes thoroughly with water.

Stop use and ask a doctor ifirritation or rash appears and lasts.

Directions

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

Other Information

Store below 110°F (43°C)

Inactive Ingredients

Water, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Fragrance, Glycerin, Isopropyl Myristate, Aloe Barbadensis Leaf Juice

Questions?

1-800-228-4722

Distributed by:
Reckitt Benckiser
Parsippany, NJ
07054-0224

PRINCIPAL DISPLAY PANEL - 59 mL Bottle Label

KILLS 99.99% OF GERMS
WITHIN 15 SECONDS*

Lysol ®
BRAND

hand
sanitizer

with Aloe
& Moisturizers

light lemon scent

2 FL. OZ. (59 mL)

3150425

LYSOL  HAND SANITIZER
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76412-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
TROLAMINE (UNII: 9O3K93S3TK)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76412-001-01	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/05/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M004	10/05/2020	12/01/2022

Labeler - Reckitt Benckiser LLC (094405024)

Establishment
Name	Address	ID/FEI	Business Operations
Precise Packaging LLC		194325999	manufacture(76412-001)

Revised: 9/2024

Document Id: 2161f94a-0461-701e-e063-6294a90a45b5

34390-5

Set id: be4dfab8-0495-4780-862d-a0836a908991

Version: 3

Effective Time: 20240905