CLOROX HAND SANITIZER- alcohol solution

Clorox Hand Sanitizer by

Drug Labeling and Warnings

Clorox Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Brand Buzz LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Alcohol 71% v/v

Purpose

Antiseptic

Use

Hand sanitizer to help decrease bacteria on skin that can potentially cause disease.

Warnings

Flammable. Keep away from fire or flame.

For external use only.

Do not use in the eyes.

Stop use and ask a doctor if

• irritation and redness develop
• condition persists for more than 72 hours

Keep out of reach of children. If swallowed, get medical help or contact a poison control center immediately.

Directions

• Spray on clean, dry hands and nails
• Wet hands thoroughly with product
• Rub hands together for no less than 15 seconds, paying particular attention to interdigital spaces, fingernails and cuticles
• Allow to dry without wiping
• Rub hands together briskly until dry

Other Information

• Store in a cool, dry place below 104 deg F (40 C)

Inactive Ingredients

Water, Isopropyl Alcohol, Glycerin, Glyceryl Laurate

Questions or Comments?

Viisit us at www.cloroxprofessional.com or call 1-888-508-4750.

Package Label: 59ml/500ml

Clorox Commercial Solutions®

CLOROX

BLEACH-FREE

Hand Sanitizer

Kills greater than 99.999%* of germs on contact

Contains hand moisturizers

Alcohol-based

*of FDA organism in the TFM for Topical Antimicrobial Drug Products

INGREDIENTS AND APPEARANCE

CLOROX HAND SANITIZER 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69540-0028
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERYL LAURATE (UNII: Y98611C087)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL ALCOHOL (UNII: ND2M416302)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69540-0028-1	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/20/2021
2	NDC: 69540-0028-4	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/20/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/20/2021

Labeler - Brand Buzz LLC (079266204)