FDA.reportPublic FDA data

Clorox Hand Sanitizer

Manufacturer
Brand Buzz LLC | Shenzhen Lantern Science Co. Ltd. | Zhejiang Guoyao Jingyue Aerosol Co., Ltd.
Effective date
2025-03-03
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:56:35

Label at a glance#

ProductClorox Hand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Dosage and administration

Squeeze gel into your palm and briskly rub hands together until dry. Children under 6 years of age should be supervised when in use.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 71% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin. Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from fire or flame.

When using this product

OTC - WHEN USING SECTION

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Discontinue use

OTC - STOP USE SECTION

if irritation and redness develop. If condition persists for more than 72 hours consult a physician.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Squeeze gel into your palm and briskly rub hands together until dry.
  • Children under 6 years of age should be supervised when in use.

Other information

SPL UNCLASSIFIED SECTION

  • Store between 15 and 30C (59 and 86F).
  • Avoid freezing and excessive heat above 40C (104F).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Extract, Carbomer, Glycerin, Tocopheryl Acetate (Vitamin E), Triethanolamine, Water (Aqua).

Package Labeling:2ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabelBoxBox

Package Labeling:500ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Package Labeling:1000ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label4Label4

Package Labeling:1000ml Refill

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2282911ethanol 71 % Topical GelPSN3
2282911ethanol 0.71 ML/ML Topical GelSCD3
2282911ethanol 71 % Topical GelSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69540-0025-12025-03-03C16284748780-1f386c649-bf1a-0266-e053-dadaa90a7c1aClorox Hand Sanitizer
69540-0025-22025-03-03C16284748780-1f386c649-bf1a-0266-e053-dadaa90a7c1aClorox Hand Sanitizer
69540-0025-32025-03-03C16284748780-1f386c649-bf1a-0266-e053-dadaa90a7c1aClorox Hand Sanitizer
69540-0025-42025-03-03C16284748780-1f386c649-bf1a-0266-e053-dadaa90a7c1aClorox Hand Sanitizer
69540-0025-12025-01-30C16284748780-1f386c649-bf1a-0266-e053-dadaa90a7c1aClorox Hand Sanitizer
69540-0025-22025-01-30C16284748780-1f386c649-bf1a-0266-e053-dadaa90a7c1aClorox Hand Sanitizer
69540-0025-32025-01-30C16284748780-1f386c649-bf1a-0266-e053-dadaa90a7c1aClorox Hand Sanitizer
69540-0025-42025-01-30C16284748780-1f386c649-bf1a-0266-e053-dadaa90a7c1aClorox Hand Sanitizer
69540-0025-12023-02-09C16284748780-1f386c649-bf1a-0266-e053-dadaa90a7c1aClorox Hand Sanitizer
69540-0025-22023-02-09C16284748780-1f386c649-bf1a-0266-e053-dadaa90a7c1aClorox Hand Sanitizer
69540-0025-32023-02-09C16284748780-1f386c649-bf1a-0266-e053-dadaa90a7c1aClorox Hand Sanitizer
69540-0025-42023-02-09C16284748780-1f386c649-bf1a-0266-e053-dadaa90a7c1aClorox Hand Sanitizer
69540-0025-12023-01-30C16284748780-1f386c649-bf1a-0266-e053-dadaa90a7c1aClorox Hand Sanitizer
69540-0025-22023-01-30C16284748780-1f386c649-bf1a-0266-e053-dadaa90a7c1aClorox Hand Sanitizer
69540-0025-32023-01-30C16284748780-1f386c649-bf1a-0266-e053-dadaa90a7c1aClorox Hand Sanitizer
69540-0025-42023-01-30C16284748780-1f386c649-bf1a-0266-e053-dadaa90a7c1aClorox Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69540-0025-1Clorox Hand Sanitizer100 in 1 BOXGEL1003
69540-0025-1Clorox Hand Sanitizer2 mL in 1 PACKETGEL23
69540-0025-2Clorox Hand Sanitizer500 mL in 1 BOTTLEGEL5003
69540-0025-3Clorox Hand Sanitizer1000 mL in 1 BOTTLEGEL10003
69540-0025-4Clorox Hand Sanitizer1000 mL in 1 BOTTLEGEL10003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69540-0025CLOROX HAND SANITIZER (ALCOHOL) GEL [BRAND BUZZ LLC]3Current NDC, Legacy NDC, 5 package rows20250305_bdd47d2f-5332-1430-e053-2a95a90a1c33.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69540-002569540-0025-1, 69540-0025-2, 69540-0025-3, 69540-0025-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
TROLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Clorox Hand SanitizerALCOHOLBrand Buzz LLCbdd47d2f-5332-1430-e053-2a95a90a1c332025-03-03WarningsExact identifier
ndc (package): 69540-0025-1
ndc (package): 69540-0025-2
ndc (package): 69540-0025-4
ndc (package): 69540-0025-3
ndc (product): 69540-0025
ndc11 (package): 69540002503
ndc11 (package): 69540002501
ndc11 (package): 69540002502
ndc11 (package): 69540002504
spl id: 2f6a3062-891e-971d-e063-6394a90a8536
spl set id: bdd47d2f-5332-1430-e053-2a95a90a1c33

Reported adverse events (FAERS/openFDA)#

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