FDA.reportPublic FDA data

Fiori Aloe Vera Hand Sanitizer

Manufacturer
International Merchandise Group | Distribuidora Cuscatlan
Effective date
2020-07-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:20:48

Label at a glance#

ProductFiori Aloe Vera Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

Keep Out of Reach Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out of Reach Children

if swallowed, get medical Help or contact a poison control center right away'

purpose

OTC - PURPOSE SECTION

To decrease bacterias on the skin that could cause disease. Recommended for repeated use.

Warning

WARNINGS SECTION

Do not Store above 105 F. may discolor some fabrics.

Harmful to wood finishes and plastics.

Flammable Keep Away from fire or flame.

Dosage Administration

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping. For children under six, use only under adult supervision. Not recomended for infants.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua/water Acrylates/c 10-30 Alkyl Acrylate Crosspolymer, Carbomer.

Aminomethyl Propanol,

Aloe Barbadensis Leaf Extract. CL19140, CI 42090

Indications for use

INDICATIONS & USAGE SECTION

For Hands external use only

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

70 % Ethyl Alcohol

package label principal

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

front and backfront and back

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
73971-19473971-194-99

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
ALCOHOL3K9958V90MACTIB
AMINOMETHYLPROPANOLLU49E6626QIACT
CARBOMER INTERPOLYMER TYPE A (55000 CPS)59TL3WG5COIACT
WATER059QF0KO0RIACT

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
d64758e0-5978-0dd6-e053-2995a90aee7caad14bc8-6fd2-2145-e053-2995a90adfaa2022-01-23WarningsExact identifier
spl set id: aad14bc8-6fd2-2145-e053-2995a90adfaa

Reported adverse events (FAERS/openFDA)#

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