FDA.reportPublic FDA data

NiTouch Hand Sanitizer

Manufacturer
Kasa Trading, Llc
Effective date
2020-09-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:29:09

Label at a glance#

ProductNiTouch Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

• Hand Sanitizer • For use when soap and water are not available.

Dosage and administration

• Apply enough product to cover hand thoroughly.  •  Rub hands together, until hands feel dry. Do not rinse. • Children under 6 years of age should be supervised when using this product.

Storage and handling

• Store below 105°F (40°C). May discolor some fabrics  • Avoid freezing and excessive heat above 105°F (40°C).

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients Ethyl Alcohol 80% (v/v)

OTC - PURPOSE SECTION

Purpose Antiseptic

Uses

INDICATIONS & USAGE SECTION

• Hand Sanitizer

• For use when soap and water are not available.

Warnings

WARNINGS SECTION

• Flammable. Keep away from fire or flame.

• For external use only.

• When using this product: Keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water. Do not inhale

   or ingest.

• Do not use in children less than 2 months of age.

• Stop use and ask a doctor if irritation or a rash develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

• Keep out of reach of children. If swallowed, get medical help and contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

• Apply enough product to cover hand thoroughly. 

• Rub hands together, until hands feel dry. Do not rinse.

• Children under 6 years of age should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

• Store below 105°F (40°C). May discolor some fabrics 

• Avoid freezing and excessive heat above 105°F (40°C).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua (Water), Glycerin, Propylene Glycol, Fragrance (Parfum), Carbomer, Triethanolamine.

SPL UNCLASSIFIED SECTION

Alcohol Gel

For external use only

Distributed by: 

Kasa Trading, LLC

4500 E. Speedway Blvd

Tucson, AZ 85712

www.kasatrading.com

Made in India

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1041498ethanol 80 % Topical GelPSN1
1041498ethanol 0.8 ML/ML Topical GelSCD1
1041498ethanol 80 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80437-001-012022-01-28C16284748780-1d6a99b39-613e-a426-e053-dadaa90af4c2Ni Touch TM HAND SANITIZER
80437-001-022022-01-28C16284748780-1d6a99b39-613e-a426-e053-dadaa90af4c2Ni Touch TM HAND SANITIZER
80437-001-032022-01-28C16284748780-1d6a99b39-613e-a426-e053-dadaa90af4c2Ni Touch TM HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80437-001-01NiTouch Hand Sanitizer1000 mL in 1 BOTTLEGEL10001
80437-001-02NiTouch Hand Sanitizer300 mL in 1 BOTTLEGEL3001
80437-001-03NiTouch Hand Sanitizer60 mL in 1 BOTTLEGEL601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80437-001NITOUCH HAND SANITIZER (ETHYL ALCOHOL) GEL [KASA TRADING, LLC]1Legacy NDC, 3 package rows20200912_d3868e70-0e35-4d1c-b414-0bbcc6ef45fd.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80437-00180437-001-03, 80437-001-02, 80437-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
TROLAMINE9O3K93S3TKIACT

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
cdad05a1-fb13-49e6-b5f8-ba7028a078f4d3868e70-0e35-4d1c-b414-0bbcc6ef45fd2020-09-09WarningsExact identifier
spl id: cdad05a1-fb13-49e6-b5f8-ba7028a078f4
spl set id: d3868e70-0e35-4d1c-b414-0bbcc6ef45fd

Reported adverse events (FAERS/openFDA)#

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