FDA.reportPublic FDA data

Handy Antibac Antiseptic Hand Sanitizing Wipes

Manufacturer
Lentus LLC
Effective date
2020-08-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:23:58

Label at a glance#

ProductHandy Antibac Antiseptic Hand Sanitizing Wipes
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only Flammable, keep away from fire or flame.

Do not use

OTC - DO NOT USE SECTION

in the eyes.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation and redness develop 
  • condition persists for more than 72 hours

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

wet hands thoroughly with product and allow to dry without wiping

Other information

SPL UNCLASSIFIED SECTION

  • Do not store above 100°F (38°C) 
  • May discolor some fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, aloe vera 

Package Labeling:10count

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Package Labeling:50count

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle2Bottle2

Package Labeling:150count

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle3Bottle3

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1307051ethanol 75 % Medicated PadPSN2
1307051ethanol 0.75 ML/ML Medicated PadSCD2
1307051ethanol 75 % Hand Sanitizer WipesSY2
1307051ethyl alcohol 75 % Topical ClothSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79873-001-002023-01-30C16284748780-1f386c649-af8e-0266-e053-dadaa90a7c1aHandy Antibac Antiseptic Hand Sanitizing Wipes
79873-001-012023-01-30C16284748780-1f386c649-af8e-0266-e053-dadaa90a7c1aHandy Antibac Antiseptic Hand Sanitizing Wipes
79873-001-022023-01-30C16284748780-1f386c649-af8e-0266-e053-dadaa90a7c1aHandy Antibac Antiseptic Hand Sanitizing Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79873-001-00Handy Antibac Antiseptic Hand Sanitizing Wipes10 in 1 PACKETCLOTH102
79873-001-00Handy Antibac Antiseptic Hand Sanitizing Wipes5 mL in 1 PATCHCLOTH52
79873-001-01Handy Antibac Antiseptic Hand Sanitizing Wipes50 in 1 PACKETCLOTH502
79873-001-01Handy Antibac Antiseptic Hand Sanitizing Wipes5 mL in 1 PATCHCLOTH52
79873-001-02Handy Antibac Antiseptic Hand Sanitizing Wipes150 in 1 PACKETCLOTH1502
79873-001-02Handy Antibac Antiseptic Hand Sanitizing Wipes5 mL in 1 PATCHCLOTH52

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79873-001HANDY ANTIBAC ANTISEPTIC HAND SANITIZING WIPES (ALCOHOL) CLOTH [LENTUS LLC]2Legacy NDC, 6 package rows20200807_450a2c7c-cb30-43e9-8b02-c0acd88e563f.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79873-00179873-001-00, 79873-001-01, 79873-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
ALCOHOL3K9958V90MACTIB

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
ac351fff-bf22-3a86-e053-2995a90a7903450a2c7c-cb30-43e9-8b02-c0acd88e563f2020-08-06WarningsExact identifier
spl id: ac351fff-bf22-3a86-e053-2995a90a7903
spl set id: 450a2c7c-cb30-43e9-8b02-c0acd88e563f

Reported adverse events (FAERS/openFDA)#

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