FDA.reportPublic FDA data

Georgette Klinger Hand Sanitizer - Lavender

Manufacturer
Alkaline Corporation
Effective date
2020-11-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:06:29

Label at a glance#

ProductGeorgette Klinger Hand Sanitizer - Lavender
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

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

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin

Warnings

WARNINGS SECTION

Flammable

Keep away from fire or flame

For external use only

OTC - WHEN USING SECTION

When using this product do not use in or near the eyes, in the case of contact rinse eyes with water.

OTC - DO NOT USE SECTION

Discontinue use if irritation or redness develops. If condition persists for more then 72 hours, consult a doctor.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Rub hands together until dry. Children under 6 years of age should be supervised when using this product.

Other Information

OTHER SAFETY INFORMATION

Store below 110°F

May discolor certain fabrics or surfaces

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Deionized Water, Peg-6, Amp-Acrylates/Vinyl Isodecanoate Crosspolymer, Glycerin, Lavandula Angustigolia (Lavender) Flower Oil

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

6 oz NDC: 80588-001-01

Georgette Klinger Hand Sanitizer - Lavender 6 ozGeorgette Klinger Hand Sanitizer - Lavender 6 oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

8 oz NDC: 80588-001-02

Georgette Klinger Hand Sanitizer - Lavender 8 ozGeorgette Klinger Hand Sanitizer - Lavender 8 oz

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
80588-00180588-001-01, 80588-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
LAVENDER OILZBP1YXW0H8IACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%)2N8MDB79NAIACT
POLYETHYLENE GLYCOL, UNSPECIFIED3WJQ0SDW1AIACT
AMINOMETHYLPROPANOLLU49E6626QIACT

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
c72a46ec-66f4-7d7e-e053-2995a90a3d67b4673231-e6cd-0fa3-e053-2a95a90aef4a2021-07-15WarningsExact identifier
spl set id: b4673231-e6cd-0fa3-e053-2a95a90aef4a

Reported adverse events (FAERS/openFDA)#

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