FDA.reportPublic FDA data

Clorox Antimicrobial

Manufacturer
Brand Buzz LLC
Effective date
2022-12-31
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:52:54

Label at a glance#

ProductClorox Antimicrobial
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

  • For handwashing to decrease bacteria on skin

Warnings

WARNINGS SECTION

For external use only.

In case of accidental ingestion, drink a glass of water to dilute. If eye contact occurs, rinse thoroughly with water. If irritation persists, contact a Poison Control Center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other Information

SPL UNCLASSIFIED SECTION

  • Avoid freezing and excessive heat above 40℃ (104℉)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Sodium Laureth Sulfate, Sodium Chlroride, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Betaine, Laureth-3, Sodium Bicarbonate, Disodium EDTA, Fragrance, Methylchloroisothiazolinone, Blue 1 (Ci 42090), Blue S Nbl (Ci 61585).

SPL UNCLASSIFIED SECTION

Do not add bleach.

Not for use in dishwashers.

PHOSPATE-FREE

BLEACH-FREE

Distributed by: Brand Buzz LLC., 1407 Broadway, New York, NY 10018

Clorox and logo are registered trademarks of the Clorox Company and are used under license by Brand Buzz LLC.
All Rights Reserved.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Clorox

Antimicrobial

HandSoap

Ultra Concentrated Dishwashing Liquid

Fresh

with Oxi

Bleach-Free

22FL OZ

(1.375 PT) 650 mL

Label

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN3
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD3
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY3
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69540-0029-12023-07-28C16284748780-10191ceaa-6fc3-198a-e063-dbdaa90aec3eClorox Antibacterial Hand Soap (Fresh)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69540-0029-1Clorox Antimicrobial650 mL in 1 BOTTLE, PLASTICSOAP6503

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69540-0029CLOROX ANTIMICROBIAL (BENZALKONIUM CHLORIDE) SOAP [BRAND BUZZ LLC]3Legacy NDC, 1 package rows20230102_c7afdaec-390f-7759-e053-2995a90aa043.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69540-002969540-0029-1

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
SODIUM LAURETH SULFATEBPV390UAP0IACT
SODIUM CHLORIDE451W47IQ8XIACT
SODIUM C14-16 OLEFIN SULFONATEO9W3D3YF5UIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
C12-14 PARETH-12M0LJS773XWIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
SODIUM BICARBONATE8MDF5V39QOIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
WATER059QF0KO0RIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
ACID BLUE 80ET8107F56DIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
f12d5ba8-7edb-ac9e-e053-2a95a90af71ec7afdaec-390f-7759-e053-2995a90aa0432022-12-31WarningsExact identifier
spl id: f12d5ba8-7edb-ac9e-e053-2a95a90af71e
spl set id: c7afdaec-390f-7759-e053-2995a90aa043

Reported adverse events (FAERS/openFDA)#

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