FDA.reportPublic FDA data

LOLA Hand Sanitizer

Manufacturer
Alyk, Inc.
Effective date
2020-11-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:05:09

Label at a glance#

ProductLOLA Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Place enough product in your palm to thoroughly cover your hands Rub hands together until dry Children under 6 years old should be supervised when using this product

Storage and handling

Use according to package label instructions Store in cool, well-ventilated place Avoid freezing or excessive heat

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 67.0% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

  • For hand sanitizing to decrease bacteria on skin
  • Recommended for repeated use

Warnings

WARNINGS SECTION

  • For external use only
  • Flammable, keep away from fire or flame

Do not use

OTC - DO NOT USE SECTION

  • Do not use internally
  • Do not use on eyes

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. If in eyes, flush thoroughly with water.

OTC - STOP USE SECTION

Discontinue use and contact a doctor if irritation and redness develop and conditions persist 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 Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product in your palm to thoroughly cover your hands
  • Rub hands together until dry
  • Children under 6 years old should be supervised when using this product

Other information

STORAGE AND HANDLING SECTION

  • Use according to package label instructions
  • Store in cool, well-ventilated place
  • Avoid freezing or excessive heat

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

59 mL NDC: 81032-411-4259 mL NDC: 81032-411-42

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81032-41181032-411-42

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
WATER059QF0KO0RIACT
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
f1ec09dd-1665-54f4-e053-2995a90ae66ab4026fcb-766d-5955-e053-2995a90ab9262023-01-10WarningsExact identifier
spl set id: b4026fcb-766d-5955-e053-2995a90ab926

Reported adverse events (FAERS/openFDA)#

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