FDA.reportPublic FDA data

Talon Antiseptic Wipes

Manufacturer
DOBOLV (QUANZHOU) PAPER CO., LTD
Effective date
2020-10-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:33:25

Label at a glance#

ProductTalon Antiseptic Wipes
Active ingredientALCOHOL, BENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

• for hand washing to decrease bacteria on the skin. • Recommended for repeat use.

Dosage and administration

• Wet hands thoroughly with product and allow to dry without rinse. • Children under six years of age should be supervised when using this product.

Storage and handling

• Store in a dry place away from fire. • Manufacturing/Expiry Date: See package for details

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% (V/V)

Benzalkonium Chloride 0.10% (W/V)

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

• for hand washing to decrease bacteria on the skin.

• Recommended for repeat use.

Warnings

WARNINGS SECTION

For external use only. Flammable.

Keep away from heat or flame.

Do not use if you have been diagnosed by a physician as being allergic to any of the ingredients.

When using this product Keep out of eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if irritation or redness develops, and if condition persists for more than 71 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children unless under adult supervision, If swallowed seek medical assistance.

Directions

DOSAGE & ADMINISTRATION SECTION

• Wet hands thoroughly with product and allow to dry without rinse.

• Children under six years of age should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

• Store in a dry place away from fire.

• Manufacturing/Expiry Date: See package for details

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Vera Extract, Betaine, Citric acid, Dodecyl polyglucoside, Glycerol, Hexadecylpyridinium Chloride, Propanediol, Sodium citrate, Vitamin E, Water(Aqua).

SPL UNCLASSIFIED SECTION

P P E CARE KIT 

MADE BY Talon®  INTERNATIONAL INC.

DISTRIBUTED BY:

Talon International, 21900 Burbank Blvd.,

Suite 101 Woodland Hills, CA 91367 USA

Made in China

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2383310benzalkonium chloride 0.1 % / ethanol 70 % Medicated PadPSN1
2383310benzalkonium chloride 1 MG/ML / ethanol 0.7 ML/ML Medicated PadSCD1
2383310benzalkonium chloride 0.1 % / ethanol 70 % Medicated PadSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d1c9d1af-bddd-448d-86f7-69052b7d5b47Product name120220627

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79891-003-102022-01-28C16284748780-1d6a99b39-b387-a426-e053-dadaa90af4c2Talon ® ANTISEPTIC WIPES

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79891-003-10Talon Antiseptic Wipes4.5 mL in 1 PACKAGECLOTH4.51
79891-003-10Talon Antiseptic Wipes10 in 1 BAGCLOTH101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79891-003TALON ANTISEPTIC WIPES (ALCOHOL, BENZALKONIUM CHLORIDE) CLOTH [DOBOLV (QUANZHOU) PAPER CO., LTD]1Legacy NDC, 2 package rows20201111_4fb9edfb-dec9-40d1-9651-e2d0db09814a.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79891-00379891-003-10

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
ALCOHOL3K9958V90MACTIB
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
ALOE VERA LEAFZY81Z83H0XIACT
BETAINE3SCV180C9WIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
LAURYL GLUCOSIDE76LN7P7UCUIACT
GLYCERINPDC6A3C0OXIACT
CETYLPYRIDINIUM CHLORIDE ANHYDROUS6BR7T22E2SIACT
PROPANEDIOL5965N8W85TIACT
SODIUM CITRATE, UNSPECIFIED FORM1Q73Q2JULRIACT
.ALPHA.-TOCOPHEROLH4N855PNZ1IACT
WATER059QF0KO0RIACT

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
1f3b792d-dd79-48e7-aacc-0de2d94b82d14fb9edfb-dec9-40d1-9651-e2d0db09814a2020-10-30WarningsExact identifier
spl id: 1f3b792d-dd79-48e7-aacc-0de2d94b82d1
spl set id: 4fb9edfb-dec9-40d1-9651-e2d0db09814a

Reported adverse events (FAERS/openFDA)#

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