Hand Sanitizer by Revlon Consumer Products Corporation / Revlon Consumer Products Corp Cutex Hand Sanitizer

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Revlon Consumer Products Corporation, Revlon Consumer Products Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HAND SANITIZER- alcohol gel 
Revlon Consumer Products Corporation

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Cutex Hand Sanitizer

Active Ingredients

Alcohol 75% v/v

Uses

Antiseptic. 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

When using this product keep out of reach of eyes, ears and mouth. In case of contact with eyes, rinse eyes throuhghly with water.

Stop Use

Stop use and ask a doctor if rash or irritation occurs. These may be signs of serious condition.

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 children under 6 years of age when using this product to avoid swallowing.

Storage

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

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

Questions?

1-800-455-6665

Inactive ingredients

Aqua/Water/Eau, Isopropyl Alcohol, Acrylates Copolymer, Glycerin, Aminomethyl Propanol, Benzophenone-3, Citric Acid, Blue 1 (Cl42090), B01266

Purpose

Antiseptic

Package

HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10967-662
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
GLYCERIN (UNII: PDC6A3C0OX)
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
WATER (UNII: 059QF0KO0R)
OXYBENZONE (UNII: 95OOS7VE0Y)
ISOPROPYL ALCOHOL (UNII: ND2M416302)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10967-662-45	250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	06/01/2020	07/14/2020

Labeler - Revlon Consumer Products Corporation (788820165)

Establishment
Name	Address	ID/FEI	Business Operations
Revlon Consumer Products Corp		809725570	manufacture(10967-662)

Revised: 1/2024

Document Id: 0ec8685b-c405-969b-e063-6294a90a0890

34390-5

Set id: a5652d5b-8511-5c89-e053-2995a90aea29

Version: 2

Effective Time: 20240112