FDA.reportPublic FDA data

Clorox Antibacterial Hand - Wild Lavender and Vanilla

Manufacturer
Brand Buzz
Effective date
2016-01-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:44:49

Label at a glance#

ProductClorox Antibacterial Hand - Wild Lavender and Vanilla
Active ingredientChloroxylenol
Label structure10 sections

Indications and uses

Helps to decrease bacteria on the skin.

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 hand soap

Uses

INDICATIONS & USAGE SECTION

  • Helps to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children, except under adult supervision. In case of accidental ingestion, drink a glass of water to dilute. If eye contact occurs, rinse thoroughly with water.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

WATER (AQUA, EAU), SODIUM LAURETH SULFATE, PEG-4 RAPESEEDAMIDE, PANTHENOL, TOCOPHERYL ACETATE, BUTYROSPERMUM PARKII (SHEA) BUTTER EXTRACT, COCOS NUCIFERA (COCONUT) FRUIT EXTRACT, COCAMIDOPROPYL BETAINE, PEG-150 DISTEARATE, POLYSORBATE 20, GLYCERIN, ASCORBIC ACID, BIOTIN, NIACINAMIDE, PROPYLENE GLYCOL, SODIUM CHLORIDE, CITRIC ACID, PEG/PPG-18/18 DIMETHICONE, SODIUM HYDROXIDE, TETRASODIUM EDTA, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, FRAGRANCE (PARFUM), EXT. VIOLET 2 (CI 60730), RED 33 (CI 17200), ALPHA-ISOMETHYL IONONE, BUTYLPHENYL METHYLPROPIONAL

Questions?

OTC - QUESTIONS SECTION

1-855-539-3564

SPL UNCLASSIFIED SECTION

Distributed by Brand Buzz LLC,
1400 Broadway, New York, NY 10018

PRINCIPAL DISPLAY PANEL - 295 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CLOROX™

antibacterial

HAND SOAP
DERMATOLOGIST TESTED

MOISTURIZING

wild lavender
& vanilla

10 FL OZ (295 mL)

Principal Display Panel - 295 mL Bottle Label
Principal Display Panel - 295 mL Bottle Label

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69540-0075-12020-01-31C16284748780-19d75b9d0-53b6-f424-e053-dadaa90a57ceClorox ™ Antibacterial Hand Soap - Wild Lavender and Vanilla

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69540-0075-1Clorox Antibacterial Hand - Wild Lavender and Vanilla295.735 mL in 1 BOTTLE, DISPENSINGSOAP295.7351

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69540-0075CLOROX ANTIBACTERIAL HAND - WILD LAVENDER AND VANILLA (CHLOROXYLENOL) SOAP [BRAND BUZZ]1Legacy NDC, 1 package rows20160201_9b6503d4-8539-4d0b-ab1f-d40c14d59250.zip

Products#

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

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69540-007569540-0075-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 27 matching rows.

Name, UNII, Kind table
NameUNIIKind
Chloroxylenol0F32U78V2QACTIB
Water059QF0KO0RIACT
Sodium Laureth-3 SulfateBPV390UAP0IACT
PEG-4 Rapeseedamide89575CN928IACT
PanthenolWV9CM0O67ZIACT
.Alpha.-Tocopherol Acetate9E8X80D2L0IACT
Sheanut OilO88E196QRFIACT
Coconut3RT3536DHYIACT
Cocamidopropyl betaine5OCF3O11KXIACT
PEG-150 Distearate6F36Q0I0ACIACT
Polysorbate 207T1F30V5YHIACT
GlycerinPDC6A3C0OXIACT
Ascorbic AcidPQ6CK8PD0RIACT
Biotin6SO6U10H04IACT
Niacinamide25X51I8RD4IACT
Propylene Glycol6DC9Q167V3IACT
Sodium Chloride451W47IQ8XIACT
Citric Acid Monohydrate2968PHW8QPIACT
PEG/PPG-18/18 Dimethicone9H0AO7T794IACT
Sodium Hydroxide55X04QC32IIACT
Edetate SodiumMP1J8420LUIACT
MethylchloroisothiazolinoneDEL7T5QRPNIACT
Methylisothiazolinone229D0E1QFAIACT
EXT. D&C Violet NO. 2G5UX3K0728IACT
D&C Red NO. 339DBA0SBB0LIACT
Isomethyl-.Alpha.-Ionone9XP4LC555BIACT
Butylphenyl MethylpropionalT7540GJV69IACT

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
fc2aaceb-3b93-41b1-af24-5c42c6b479099b6503d4-8539-4d0b-ab1f-d40c14d592502016-01-05WarningsExact identifier
spl id: fc2aaceb-3b93-41b1-af24-5c42c6b47909
spl set id: 9b6503d4-8539-4d0b-ab1f-d40c14d59250

Reported adverse events (FAERS/openFDA)#

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