FDA.reportPublic FDA data

Hyatt Hand Sanitizer 70% Alcohol

Manufacturer
Hunter Amenities International Limited | KIMIRICA HUNTER INTERNATIONAL LLP
Effective date
2022-01-06
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:18:55

Label at a glance#

ProductHyatt Hand Sanitizer 70% Alcohol
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

Antiseptic (skin) cleanser Medicated (skin) cleanser Antibacterial (skin) cleanser Kills harmful bacteria/germs Effective in destroying (harmful) bacteria to provide antiseptic cleansing For perosnal hand hygine to help prevent the spread of bacteria

Dosage and administration

Adults and children over 2 years: For occasional and personal domestic use. Supervise children when they use this product. Rub thoroughly into hands for at least 30 seconds. Allow to dry.

Label contents#

Full prescribing information#

Active ingredient (v/v)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70.0 %

Purpose

OTC - PURPOSE SECTION

Antiseptic skin cleanser

Uses

INDICATIONS & USAGE SECTION

  • Antiseptic (skin) cleanser
  • Medicated (skin) cleanser
  • Antibacterial (skin) cleanser
  • Kills harmful bacteria/germs
  • Effective in destroying (harmful) bacteria to provide antiseptic cleansing
  • For perosnal hand hygine to help prevent the spread of bacteria

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask/ consult a doctor/ physician/ health care practitioner/ health care provider/ health care professional if

OTC - STOP USE SECTION

irritation develops.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

if swallowed, call a Poison Control Center or get medical help right away.

Flammability warning.

SPL UNCLASSIFIED SECTION

Keep away from open flame and sources of heat.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children over 2 years:

  • For occasional and personal domestic use.
  • Supervise children when they use this product.
  • Rub thoroughly into hands for at least 30 seconds. Allow to dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua/Water/Eau, Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Aloe Barbadensis Leaf Extract, Avena Sativa Kernal Extract, PEG-40 Hydrogenated Castor Oil, Tocopherol Acetate.

Questions?

OTC - QUESTIONS SECTION

1-800-668-1483

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
65910-01565910-015-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
TROLAMINE9O3K93S3TKIACT
ALOE VERA LEAFZY81Z83H0XIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
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
e8064928-0f7b-04b4-e053-2a95a90a974c9ba0a549-2143-4723-811e-e62d7fb931272022-09-06WarningsExact identifier
spl set id: 9ba0a549-2143-4723-811e-e62d7fb93127

Reported adverse events (FAERS/openFDA)#

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