FDA.reportPublic FDA data

Everwipe Antibacterial

Manufacturer
Brands International Corporation
Effective date
2021-04-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:39:45

Label at a glance#

ProductEverwipe Antibacterial
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride - 0.13%

OTC - PURPOSE SECTION

Purpose: Antibacterial

INDICATIONS & USAGE SECTION

Effective in destroying bacteria to provide antiseptic cleaning.

DOSAGE & ADMINISTRATION SECTION

Direction

  • wet hands
  • apply palmful to hands
  • scrub thoroughly
  • rinse

WARNINGS SECTION

For external use only

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops

OTC - WHEN USING SECTION

When using this product

  • do not get it into eyes. If contact occurs, rinse eye thoroughly with water

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

INACTIVE INGREDIENT SECTION

Lauramidopropylamine oxide, Lauryl glucoside, PEG-150 distearate, Glycol Stearate, Perfume, Aloe extract, Tocopheryl Acetate, Peg 7- Glyceryl Cocoate, Cetrimonium, Chloride, Citric Acid, Glycerin, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN1
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD1
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY1
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50157-264-432025-01-30C16284748780-12cef2736-716e-d83d-e063-dadaa90ab31fEverwipe Antibacterial Hand Soap

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50157-264-43Everwipe Antibacterial443 mL in 1 BOTTLE, PLASTICLIQUID4431

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50157-264EVERWIPE ANTIBACTERIAL (BENZALKONIUM CHLORIDE) LIQUID [BRANDS INTERNATIONAL CORPORATION]1Legacy NDC, 1 package rows20210417_c01ca3ae-8c20-c73c-e053-2a95a90afe58.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50157-26450157-264-43

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
LAURYL GLUCOSIDE76LN7P7UCUIACT
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
GLYCERINPDC6A3C0OXIACT
DITETRACYCLINE TETRASODIUM EDETATEWX0A0IT7K5IACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
PEG-7 GLYCERYL COCOATEVNX7251543IACT
PEG-150 DISTEARATE6F36Q0I0ACIACT
GLYCOL STEARATE0324G66D0EIACT
LAURAMIDOPROPYLAMINE OXIDEI6KX160QTVIACT

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
c01c93b1-dbcb-40e6-e053-2a95a90ad262c01ca3ae-8c20-c73c-e053-2a95a90afe582021-04-16WarningsExact identifier
spl id: c01c93b1-dbcb-40e6-e053-2a95a90ad262
spl set id: c01ca3ae-8c20-c73c-e053-2a95a90afe58

Reported adverse events (FAERS/openFDA)#

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