Kiehls Since 1851 Clean Strength Antiseptic Hand Sanitizer by L'Oreal USA Products Inc Drug Facts

Kiehls Since 1851 Clean Strength Antiseptic Hand Sanitizer by

Drug Labeling and Warnings

Kiehls Since 1851 Clean Strength Antiseptic Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by L'Oreal USA Products Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

KIEHLS SINCE 1851 CLEAN STRENGTH ANTISEPTIC HAND SANITIZER- alcohol gel 
L'Oreal USA Products 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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Drug Facts

Active ingredient

Alcohol 71% v/v

Purpose

Antiseptic

Use

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 fire or heat.

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 appears and lasts

Keep out of reach of children.

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

Directions

• place enough product on hands to cover all surfaces. Rub hands together until dry.
• supervise chlildren under 6 years of age when using this product to avoid swallowing

Other information

● store between 15°- 30°C (59° - 86°F)
● avoid freezing and excessive heat above 40°C (104°F)

Inactive ingredients

water, glycerin, polyacryloyldimethyl taurate, eucalyptus globulus leaf oil, rosmarinus officinalis (rosemary) leaf oil, limonene, linalool

Questions or comments?

Call toll free 1-800-946-4453

KIEHLS SINCE 1851 CLEAN STRENGTH ANTISEPTIC HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49967-998
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	71 L  in 100 L

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
AMMONIUM POLYACRYLOYLDIMETHYL TAURATE (55000 MPA.S) (UNII: F01RIY4371)
EUCALYPTUS OIL (UNII: 2R04ONI662)
ROSEMARY OIL (UNII: 8LGU7VM393)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
LINALOOL, (+/-)- (UNII: D81QY6I88E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49967-998-01	0.120 L in 1 TUBE; Type 0: Not a Combination Product	02/01/2021	06/02/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/01/2021	06/02/2023

Labeler - L'Oreal USA Products Inc (002136794)

Establishment
Name	Address	ID/FEI	Business Operations
L'Oreal USA Products Inc		624244349	manufacture(49967-998)

Revised: 6/2022

Document Id: a405da3d-c805-4502-ad51-4cb9b6b15b7a

34390-5

Set id: 68848e9d-8de0-4ed3-9eb0-bf7a8df1de6d

Version: 2

Effective Time: 20220630