UTUA Hand Sanitizer with Moisturizers

Manufacturer
ShangHai Genting Cosmetics Co.,Ltd.
Effective date
2020-06-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:27:50

Label at a glance#

ProductUTUA Hand Sanitizer with Moisturizers
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

For hand washing to help reduce bacteria that potentially can cause disease. Recommended for repeated use. For use when soap and water are not available.

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Children under 6 years of age should be supervied by adult when applying this product.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • For hand washing to help reduce bacteria that potentially can cause disease. Recommended for repeated use. For use when soap and water are not available.

Warnings

WARNINGS SECTION

  • For external use only.
  • Flammable.
  • Keep away from heat or flame.

Do not use

OTC - DO NOT USE SECTION

  • In children less than 2 months of age.
  • On open skin wounds.

When using this product

OTC - WHEN USING SECTION

do not use in or near eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or rash appears on the skin.

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

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Children under 6 years of age should be supervied by adult when applying this product.

Other information

SPL UNCLASSIFIED SECTION

  • Store between 15-30°C (59-86°F).
  • Avoid freezing and excessive heat above 40°C(104°F).
  • May discolor some fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aminomethyl propanol, Aloe barbadensis leaf juice, Butylene glycol, Carbomer, Flavor, Glycerin, Hydrolyzed yaluronate, Propylene glycol, PEG/PPG-17/6 copolymer, PEG-40 hydrogenated castor oil, Trehalose, Water

Package Labeling : 60ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling : 300ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Package Labeling : 500ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

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
75075-00075075-000-02, 75075-000-10, 75075-000-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
0b250ca1-a6a7-255d-e063-6294a90ad2aca746bfab-56d5-4a87-e053-2995a90ac0502023-11-27WarningsExact identifier
spl set id: a746bfab-56d5-4a87-e053-2995a90ac050

Reported adverse events (FAERS/openFDA)#

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