HAND SANITIZER

Manufacturer
TOUCHLAND LLC
Effective date
2024-12-05
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 20:47:33

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

■ FOR HAND WASHING TO DECREASE BACTERIA ON THE SKIN ■ RECOMMENDED FOR REPEATED USE

Dosage and administration

place enough product in your palms to thoroughly cover your hands children under the age of 6 years of age should be supervised when using this product rub hands together briskly until dry

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL 67%

PURPOSE

OTC - PURPOSE SECTION

ANTISEPTIC

USES

INDICATIONS & USAGE SECTION

■ FOR HAND WASHING TO DECREASE BACTERIA ON THE SKIN

■ RECOMMENDED FOR REPEATED USE

WARNINGS

WARNINGS SECTION

For external use only.

Flammable, Keep away from fire or flame.

Do not usein or near the eyes • In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if• irritation or redness develops •condition persists for more than 72 hours.

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

  • place enough product in your palms to thoroughly cover your hands
  • children under the age of 6 years of age should be supervised when using this product
  • rub hands together briskly until dry

Other Information

OTHER SAFETY INFORMATION

• protect the product in the container from excessive heat and direct sun

• store below 104°F (40°C) •may discolor certain favrics

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, Aloe Vera Leaf Juice, Radish Root Ferment Filtrate, Glycereth-26, Lime (Citrus Aurantifolia) Seed Oil, Lemon (Citrus Limon) Peel Oil, Limonene

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL (PDP)_ReFeel01b LBL (PDP)_ReFeel

01b LBL (DF box)_ReFeel01b LBL (DF box)_ReFeel

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72033-40872033-408-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
2884ab76-1407-bf15-e063-6394a90acb83e4bc0f12-a735-912c-e053-2995a90ada332024-12-05WarningsExact identifier
spl id: 2884ab76-1407-bf15-e063-6394a90acb83
spl set id: e4bc0f12-a735-912c-e053-2995a90ada33

Reported adverse events (FAERS/openFDA)#

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