NiTouch Alcohol Gel Hand Sanitizer

Manufacturer
Kasa Trading, Llc
Effective date
2020-09-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:30:28

Label at a glance#

ProductNiTouch Alcohol Gel 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 75% (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, DiPropylene Glycol, Fragrance, Carbomer, Triethanolamine.

SPL UNCLASSIFIED SECTION

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

PackagingPackagingPackagingPackagingPackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN1
1305100ethanol 0.75 ML/ML Topical GelSCD1
1305100ethanol 75 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80437-003-01NiTouch Alcohol Gel Hand Sanitizer1000 mL in 1 BOTTLEGEL10001
80437-003-02NiTouch Alcohol Gel Hand Sanitizer300 mL in 1 BOTTLEGEL3001
80437-003-03NiTouch Alcohol Gel Hand Sanitizer60 mL in 1 BOTTLEGEL601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80437-003NITOUCH ALCOHOL GEL HAND SANITIZER (ETHYL ALCOHOL) GEL [KASA TRADING, LLC]1Legacy NDC, 3 package rows20200929_e6cbaf20-87a0-41df-a197-f95182217344.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
80437-00380437-003-03, 80437-003-02, 80437-003-01

Ingredients#

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

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

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
68d5382a-f8bb-491b-8f2e-0b8f7a59fbece6cbaf20-87a0-41df-a197-f951822173442020-09-25WarningsExact identifier
spl id: 68d5382a-f8bb-491b-8f2e-0b8f7a59fbec
spl set id: e6cbaf20-87a0-41df-a197-f95182217344

Reported adverse events (FAERS/openFDA)#

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