FDA.reportPublic FDA data

Touchland Applicious Hand Sanitizer Spray

Manufacturer
Bell International Laboratories, Inc
Effective date
2021-08-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:38:46

Label at a glance#

ProductApplelicious
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

to decrease bacteria on the skin recommended for repeated use

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • 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 use in or near the eyes. In case of contact, rinse eye thoroughly with water. Avoid contact with broken skin

Stop use and ask a doctor if

  • irritation and redness develop
  • 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 palm to thoroughly cover your hands
  • children under 6 years of age shoud be supervised when using this product
  • rub hands together briskly until dry

Other Information

OTHER SAFETY INFORMATION

  • protect this product in this container from excessive heat and direct sun
  • Store below 104 F (40 C)
  • may discolor certain fabrics

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Aloe Barbadensis Leaf Juice, Leuconostoc/Radish Root Ferment Lysate Filtrate, Glycereth-26, Citrus Limon (Lemon) Peel Oil, Citrus Aurantifolia (Lime) Oil, Fragrance, Yellow 5, Yellow 6, Blue 1

pouch label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

pouchpouch

back

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

backback

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76150-27276150-272-51

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
LEUCONOSTOC/RADISH ROOT FERMENT FILTRATED2QHA03458IACT
FD&C YELLOW NO. 6H77VEI93A8IACT
FD&C YELLOW NO. 5I753WB2F1MIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
LEMON OILI9GRO824LLIACT
GLYCERETH-26NNE56F2N14IACT
LIME OILUZH29XGA8GIACT
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
c8e8701c-e6e2-085c-e053-2995a90a0849c8e8701c-e6e1-085c-e053-2995a90a08492021-08-06WarningsExact identifier
spl id: c8e8701c-e6e2-085c-e053-2995a90a0849
spl set id: c8e8701c-e6e1-085c-e053-2995a90a0849

Reported adverse events (FAERS/openFDA)#

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