FDA.reportPublic FDA data

Jafra Daily Advanced Hand Sanitizer

Manufacturer
Jafra Cosmetics International Inc | Distribuidora Comercial Jafra, S.A. de C.V.
Effective date
2022-05-11
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:01:20

Label at a glance#

ProductJafra Daily Advanced Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

To help reduce bacteria on the skin

Dosage and administration

Put enough hand sanitizer in your palm to cover hands and rub hands together until dry. Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% w/v. 

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • To help reduce bacteria on the skin

Warnings

WARNINGS SECTION

For external use only.
Flammable. Keep away from source of heat or flame.
When using this product Avoid contact with eyes. If contact occurs, rinse thoroughly with water.
Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Put enough hand sanitizer in your palm to cover hands and rub hands together until dry.
  • Children under 6 years of age should be supervised when using this product.

Other information

SPL UNCLASSIFIED SECTION

  • Store at a temperature below 110°F (43°C)
  • May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Carbomer, Glycerin, Triethanolamine, Water/Aqua

Product labels

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

image descriptionimage description

image descriptionimage description

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68828-75668828-756-01, 68828-756-02

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
TROLAMINE9O3K93S3TKIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
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
014f6cad-7e81-36a2-e063-6294a90acd6947de115c-be04-4002-84ee-873fe54ad3842023-07-25WarningsExact identifier
spl set id: 47de115c-be04-4002-84ee-873fe54ad384

Reported adverse events (FAERS/openFDA)#

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