FDA.reportPublic FDA data

PERFECT CARE Citrus HAND SANITIZER

Manufacturer
Handock Cosmetics Co., Ltd.
Effective date
2021-02-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:53:47

Label at a glance#

ProductPERFECT CARE Citrus HAND SANITIZER
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Hand sanitizer to help reduce bacteria on the skin. Recommended for repeated use.

Dosage and administration

Put enough product in your palm and rub hands together until dry. For children under 6 years, use only under adult supervision.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Ethanol 70%(v/v)

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, Propylene Glycol, Glycerin, Triethanolamine, Carbomer, Fragrance

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

WARNINGS

WARNINGS SECTION

For external use only. Flammable.
Keep away from flame and fire.

When using this product
Keep out of eyes.
In case of contact, rinse eyes thoroughly with water.


Stop use and ask a doctor if
irritation or redness develops and lasts.

Keep out of reach of children
If swallowed, get medical help or contact a Poison Control Center right away.

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.

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin.
Recommended for repeated use.

Directions

DOSAGE & ADMINISTRATION SECTION

Put enough product in your palm and rub hands together until dry.
For children under 6 years, use only under adult supervision.

Other information

OTHER SAFETY INFORMATION

Store below 110°F (43°C).
May discolor some fabrics or surfaces.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottleImage of bottle

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
76369-813076369-8130-1

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
Propylene Glycol6DC9Q167V3IACT
GlycerinPDC6A3C0OXIACT
TROLAMINE9O3K93S3TKIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT

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
ebd1da6e-76c4-4314-b9d0-4f687d150285dbedc707-2d10-4c39-bb18-392d310bd67b2023-04-07WarningsExact identifier
spl set id: dbedc707-2d10-4c39-bb18-392d310bd67b

Reported adverse events (FAERS/openFDA)#

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