FDA.reportPublic FDA data

equate

Manufacturer
Walmart | Apotex Inc. | Ningbo Liyuan Daily Chemical Products Co., Ltd.
Effective date
2017-11-29
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:53:09

Label at a glance#

Productequate
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

Use hand sanitizer to help reduce bacteria on skin. Directions Wet hands thoroughly with product and rub into skin until dry.  Children under 6 ears of age should be supervised by an adult when using.

Dosage and administration

Use hand sanitizer to help reduce bacteria on skin. Directions Wet hands thoroughly with product and rub into skin until dry.  Children under 6 ears of age should be supervised by an adult when using.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water (Agua), Cetrimonium Chloride, Glycerine, Tetrasodium EDTA, Fragrance, Dimehicone, Disodium Cocoamphodiacetate, Aloe Barbadensis Leaf Extract, Citric Acid.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses AND Directions

INDICATIONS & USAGE SECTION

Use hand sanitizer to help reduce bacteria on skin.

Directions

Wet hands thoroughly with product and rub into skin until dry.  Children under 6 ears of age should be supervised by an adult when using.

Warnings

WARNINGS SECTION

For external use only.

Flammable Keep away from heat and flame.  Do not store 104o ​F/40​o ​C

Keep out of reach of children.  If swallowed get medical help or contact a Poison Control Center right away. (1-800-222-1222)

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

When using

OTC - WHEN USING SECTION

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

Stop use

OTC - STOP USE SECTION

Stop use and ask doctor if irritation or redness develops.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and rub into skin until dry.  Children under 6 years of age should be supervised by an adult when using.

PRINCIPAL DISPLAY PANEL – Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

equate Beauty                NDC 49035-591-01

Foaming Hand Sanitizer

Aloe

2 FL oz. (59mL)

Satisfaction guaranteed - For questions or comments please call 1-888-287-1915

DISTRIBUTED BY: Wal-Mart Stores, Inc.

Bentonville, AR 72716

PRODUCT OF CHINA

EQUATE BEAUTY PDP LABELEQUATE BEAUTY PDP LABEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1049254benzalkonium chloride 0.13 % Topical SolutionPSN2
1049254benzalkonium chloride 1.3 MG/ML Topical SolutionSCD2
1049254benzalkonium chloride 0.13 % Topical SolutionSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49035-591-012024-01-30C16284748780-11030e365-6245-111a-e063-dadaa90a10e2DRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49035-591-01equate59 mL in 1 BOTTLE, PLASTICLIQUID592

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49035-591EQUATE (BENZALKONIUM CHLORIDE) LIQUID [WALMART]2Legacy NDC, 1 package rows20171130_f5895869-dca5-4fc9-9de8-aa52accc468d.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49035-59149035-591-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
GLYCERINPDC6A3C0OXIACT
EDETATE SODIUMMP1J8420LUIACT
DIMETHICONE92RU3N3Y1OIACT
DISODIUM COCOAMPHODIACETATE18L9G3U51MIACT
ALOE VERA LEAFZY81Z83H0XIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT

Source Document#

Source XML · Source PDF

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
aa3bcadd-fd45-4f40-9539-6c91bed4c391f5895869-dca5-4fc9-9de8-aa52accc468d2017-11-29WarningsExact identifier
spl id: aa3bcadd-fd45-4f40-9539-6c91bed4c391
spl set id: f5895869-dca5-4fc9-9de8-aa52accc468d

Reported adverse events (FAERS/openFDA)#

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