Clorox Antibacterial

Manufacturer
Brand Buzz
Effective date
2021-07-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:41:39

Label at a glance#

ProductClorox Antibacterial
Active ingredientCHLOROXYLENOL
Label structure10 sections

Dosage and administration

Apply onto wet hands, lather for at least 30 seconds and rinse thoroughly.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

DRUG FACTS

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Chloroxylenol 0.3%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

  • for handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

When using this product avoid contact with the eyes. If contact occurs, rinse eyes with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops and 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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply onto wet hands, lather for at least 30 seconds and rinse thoroughly.

Inactive ingredients

INACTIVE INGREDIENT SECTION

WATER, SODIUM LAURETH SULFATE, COCAMIDOPROPYL BETAINE, GLYCERIN, COCAMIDE METHYL MEA, SODIUM CHLORIDE, PARFUM, CHLOROXYLENOL, CITRIC ACID, DISODIUM EDTA, METHYLCHLOROISOTHIAZOLINONE AND METHYLISOTHIAZOLINONE, DYE.

Questions or Comments?

OTC - QUESTIONS SECTION

Call us at 1-888-508-4750 or visit us at www.brandbuzzcp.com

SPL UNCLASSIFIED SECTION

Clorox Antibacterial Hand Soap washes away dirt and bacteria from hands. This gentle antibacterial hand soap is perfect for frequent handwahing and leaves a fresh smelling scent.

Developed in USA

Responsibly Made in China ©2021

Distributed by Brand Buzz LLC,

1407 Broadway, New York, NY 10018

The Clorox name and logo are registered trademarks of The Clorox Company and are used under license by Brand Buzz LLC.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CLOROX™

Antibacterial

Hand Soap

Citrus Blast

Bleach-Free

16 fl. oz. (1pt) 473ml

473473

34 fl oz. (1L)

1L1L

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
413261chloroxylenol 0.3 % Medicated Liquid SoapPSN1
413261chloroxylenol 3 MG/ML Medicated Liquid SoapSCD1
413261chloroxylenol 0.3 % Medicated Liquid SoapSY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69540-0034-1Clorox Antibacterial473 mL in 1 BOTTLE, PLASTICSOAP4731
69540-0034-2Clorox Antibacterial1000 mL in 1 BAGSOAP10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69540-0034CLOROX ANTIBACTERIAL (CHLOROXYLENOL) SOAP [BRAND BUZZ]1Legacy NDC, 2 package rows20210724_f8137bc2-87c7-4ec9-a7b3-be4f1bfb29e3.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69540-003469540-0034-1, 69540-0034-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

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
c7cd90db-cfdb-ef8b-e053-2995a90aeb9cf8137bc2-87c7-4ec9-a7b3-be4f1bfb29e32021-07-23WarningsExact identifier
spl id: c7cd90db-cfdb-ef8b-e053-2995a90aeb9c
spl set id: f8137bc2-87c7-4ec9-a7b3-be4f1bfb29e3

Reported adverse events (FAERS/openFDA)#

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