FDA.reportPublic FDA data

Carroll Ultrex Antimicrobial Wipes

Manufacturer
Carroll Company
Effective date
2018-01-31
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-05-31 22:54:19

Label at a glance#

ProductCarroll Ultrex Antimicrobial Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

for hand cleaning to decrease bacteria on the skin kills 99.9% of most common germs

Dosage and administration

Use textured side of wipe to clean hands wet hands thoroughly with product allow to dry without rinsing

Storage and handling

store at room temperature

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13% w/w

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • for hand cleaning to decrease bacteria on the skin
  • kills 99.9% of most common germs

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

  • do not use in or near eyes
  • discontinue use if irritation and redness develop

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Use textured side of wipe to clean hands
  • wet hands thoroughly with product
  • allow to dry without rinsing

Other information

STORAGE AND HANDLING SECTION

  • store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, 2-Phenoxyethanol, Alkylpolyglucoside, C 8-10,C10-16, Fragrance, Lauramine,N,N-dimethyl, N-oxide, Tocopherol acetate, Aloe barbadensis leaf juice, PEG-40 Lanolin, Tetrasodium EDTA, Methylchloroisothiazoline, Methylisothiazoline.

SPL UNCLASSIFIED SECTION

Manufactured in the U.S.A. by:
CARROLL ® COMPANY
2900 W. Kingsley Rd., Garland, Texas 75041

PRINCIPAL DISPLAY PANEL - 70 Cloth Canister Label WIPES CARROLL® ULTREX Antimicrobial Wipes -Kills 99.9% of common germs -Contains Aloe and Vitamin E -Moisturizes and conditions skin -Alcohol free CITRUS SCENTED Dual Textured Wipe KEEP OUT OF REACH OF CHILD...

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038558benzalkonium chloride 0.13 % Medicated PadPSN6
1038558benzalkonium chloride 1.3 MG/ML Medicated PadSCD6
1038558benzalkonium chloride 0.13 % Topical ClothSY6
1038558benzalkonium chloride 0.13 % Topical SwabSY6
1038558benzalkonium chloride 0.13 GM per 100 GM Topical PadSY6
1038558benzalkonium chloride 0.13 GM per 100 GM Topical SwabSY6
1038558benzalkonium chloride 1 ML per 750 ML Topical SwabSY6

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130074948005816GTIN-13: 0074948005816
EAN-13: 0074948005816
GTIN-12: 074948005816
UPC-A: 074948005816
GTIN storage (14 digits): 00074948005816		10685-681.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10685-681-972020-01-31C16284748780-19d75b9d0-688c-f424-e053-dadaa90a57ceCarroll ® Ultrex Antimicrobial Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10685-681-97Carroll Ultrex Antimicrobial Wipes70 in 1 CANISTERCLOTH706

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10685-681CARROLL ULTREX ANTIMICROBIAL WIPES (BENZALKONIUM CHLORIDE) CLOTH [CARROLL COMPANY]6Legacy NDC, 1 package rows20180131_d3ab381d-a4ea-43d9-945c-f90c058b1806.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Benzalkonium ChlorideACTIVE INGREDIENTF5UM2KM3W74
BenzalkoniumACTIVE MOIETY7N6JUD5X6Y4
.Alpha.-Tocopherol acetateINACTIVE INGREDIENT9E8X80D2L04
Aloe Vera LeafINACTIVE INGREDIENTZY81Z83H0X4
Decyl GlucosideINACTIVE INGREDIENTZ17H97EA6Y4
Edetate SodiumINACTIVE INGREDIENTMP1J8420LU4
Lauramine OxideINACTIVE INGREDIENT4F6FC4MI8W4
MethylchloroisothiazolinoneINACTIVE INGREDIENTDEL7T5QRPN4
MethylisothiazolinoneINACTIVE INGREDIENT229D0E1QFA4
PhenoxyethanolINACTIVE INGREDIENTHIE492ZZ3T4
WaterINACTIVE INGREDIENT059QF0KO0R4

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10685-68110685-681-97

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
PHENOXYETHANOLHIE492ZZ3TIACT
DECYL GLUCOSIDEZ17H97EA6YIACT
LAURAMINE OXIDE4F6FC4MI8WIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALOE VERA LEAFZY81Z83H0XIACT
EDETATE SODIUMMP1J8420LUIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

Source Document#

Source XML · Source PDF

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 23 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TCREAM / TOPICAL57 mgExact identifier — unii candidate
6 equally ranked IID candidates
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TAEROSOL, FOAM / TOPICAL72 mgExact identifier — unii candidate
6 equally ranked IID candidates
Lauramine OxideLAURAMINE OXIDE4F6FC4MI8WSPONGE / TOPICALNAExact identifier — unii candidate
2 equally ranked IID candidates
.Alpha.-Tocopherol acetate.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0CAPSULE / ORAL2 mgExact identifier — unii candidate
3 equally ranked IID candidates
Edetate SodiumEDETATE SODIUMMP1J8420LUSOLUTION / TOPICAL0.3 %w/wExact identifier — unii candidate
12 equally ranked IID candidates
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TAEROSOL / TOPICAL1.05 %w/wExact identifier — unii candidate
6 equally ranked IID candidates
Edetate SodiumEDETATE SODIUMMP1J8420LUCAPSULE / ORAL1 mgExact identifier — unii candidate
12 equally ranked IID candidates
Edetate SodiumEDETATE SODIUMMP1J8420LUSOAP / TOPICAL0.12 %w/wExact identifier — unii candidate
12 equally ranked IID candidates
Edetate SodiumEDETATE SODIUMMP1J8420LUSOLUTION / OPHTHALMIC0.1 %w/vExact identifier — unii candidate
12 equally ranked IID candidates
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TLOTION / TOPICAL1 %w/wExact identifier — unii candidate
6 equally ranked IID candidates
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TGEL / TOPICAL14 mgExact identifier — unii candidate
6 equally ranked IID candidates
Edetate SodiumEDETATE SODIUMMP1J8420LUINJECTION / INTRAMUSCULAR0.01 %w/vExact identifier — unii candidate
12 equally ranked IID candidates
Edetate SodiumEDETATE SODIUMMP1J8420LUTABLET / ORAL5 mgExact identifier — unii candidate
12 equally ranked IID candidates
.Alpha.-Tocopherol acetate.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0FILM / BUCCAL0.09 mgExact identifier — unii candidate
3 equally ranked IID candidates
Edetate SodiumEDETATE SODIUMMP1J8420LUINJECTION / INTRAVENOUS0.01 %w/vExact identifier — unii candidate
12 equally ranked IID candidates
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TCREAM, AUGMENTED / TOPICAL10 mgExact identifier — unii candidate
6 equally ranked IID candidates
Lauramine OxideLAURAMINE OXIDE4F6FC4MI8WSOLUTION / TOPICAL3.5 %w/vExact identifier — unii candidate
2 equally ranked IID candidates
.Alpha.-Tocopherol acetate.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0TABLET / ORAL0.5 mgExact identifier — unii candidate
3 equally ranked IID candidates
Edetate SodiumEDETATE SODIUMMP1J8420LUEMULSION / OPHTHALMIC0.02 %w/vExact identifier — unii candidate
12 equally ranked IID candidates
Edetate SodiumEDETATE SODIUMMP1J8420LUSHAMPOO / TOPICAL1.33 %w/wExact identifier — unii candidate
12 equally ranked IID candidates
Edetate SodiumEDETATE SODIUMMP1J8420LUSPONGE / TOPICAL0.14 %w/wExact identifier — unii candidate
12 equally ranked IID candidates
Edetate SodiumEDETATE SODIUMMP1J8420LUINJECTION, SOLUTION / INTRAVENOUS0.04 %w/vExact identifier — unii candidate
12 equally ranked IID candidates
Edetate SodiumEDETATE SODIUMMP1J8420LULOTION / TOPICAL0.17 %w/wExact identifier — unii candidate
12 equally ranked IID candidates

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
641704f3-7e7a-73d3-e053-2991aa0af008d3ab381d-a4ea-43d9-945c-f90c058b18062018-01-31WarningsExact identifier
spl id: 641704f3-7e7a-73d3-e053-2991aa0af008
spl set id: d3ab381d-a4ea-43d9-945c-f90c058b1806

Reported adverse events (FAERS/openFDA)#

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