Clorox Hand Sanitizer

Manufacturer: Brand Buzz LLC
Effective date: 2023-02-02
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:53:56

Label at a glance#

ProductClorox Hand Sanitizer

Active ingredientALCOHOL

Label structure9 sections

Dosage and administration

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

Contacts and useful links#

PhoneLabel contact1-888-508-4750

Websitewww.cloroxprofessional.com

www.cloroxprofessional.com

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 71% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only.

OTC - DO NOT USE SECTION

Do not use in the eyes.

OTC - STOP USE SECTION

Stop use and ask a doctor if

irritation and redness develop
condition persists for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

SPL UNCLASSIFIED SECTION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Isopropyl Alcohol, Glycerin, Glyceryl Laurate

Questions or Comments?

OTC - QUESTIONS SECTION

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

Package Label: 59ml/500ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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

Principal Display Panel Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
69540-0028-1	2025-01-30	C162847	48780-1	f386c649-caf7-0266-e053-dadaa90a7c1a	Clorox Hand Sanitizer (Bleach-Free)
69540-0028-4	2025-01-30	C162847	48780-1	f386c649-caf7-0266-e053-dadaa90a7c1a	Clorox Hand Sanitizer (Bleach-Free)
69540-0028-1	2023-02-09	C162847	48780-1	f386c649-caf7-0266-e053-dadaa90a7c1a	Clorox Hand Sanitizer (Bleach-Free)
69540-0028-4	2023-02-09	C162847	48780-1	f386c649-caf7-0266-e053-dadaa90a7c1a	Clorox Hand Sanitizer (Bleach-Free)
69540-0028-1	2023-01-30	C162847	48780-1	f386c649-caf7-0266-e053-dadaa90a7c1a	Clorox Hand Sanitizer (Bleach-Free)
69540-0028-4	2023-01-30	C162847	48780-1	f386c649-caf7-0266-e053-dadaa90a7c1a	Clorox Hand Sanitizer (Bleach-Free)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
69540-0028-1	Clorox Hand Sanitizer	59 mL in 1 BOTTLE, SPRAY	SOLUTION	59		2
69540-0028-4	Clorox Hand Sanitizer	500 mL in 1 BOTTLE, PUMP	SOLUTION	500		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69540-0028	CLOROX HAND SANITIZER (ALCOHOL) SOLUTION [BRAND BUZZ LLC]	2	Legacy NDC, 2 package rows	20230211_c06c238d-bdb4-759f-e053-2995a90ab51e.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

Clorox Hand Sanitizer
Alcohol
WATER
GLYCERYL LAURATE
GLYCERIN
ISOPROPYL ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
69540-0028	69540-0028-1, 69540-0028-4

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
GLYCERYL LAURATE	Y98611C087	IACT
GLYCERIN	PDC6A3C0OX	IACT
ISOPROPYL ALCOHOL	ND2M416302	IACT
ALCOHOL	3K9958V90M	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
f3bf0eb2-f1f7-2b17-e053-2a95a90a747e			c06c238d-bdb4-759f-e053-2995a90ab51e	2023-02-02	Warnings	Exact identifier spl id: f3bf0eb2-f1f7-2b17-e053-2a95a90a747e spl set id: c06c238d-bdb4-759f-e053-2995a90ab51e

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.