Fiori Aloe Vera Hand Sanitizer

Manufacturer
International Merchandise Group | Distribuidora Cuscatlan
Effective date
2020-11-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:07:07

Label at a glance#

ProductFiori Aloe Vera Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Label contents#

Full prescribing information#

WARNINGS SECTION

Do Not STORE ABOVE 105oF MAY DISCOLOR SOME FABRICS.

FOR EXTERNAL UUSE ONLY

FLAMMABLE , KEEP AWAY FROM FIRE OR FLAME

WHEN USING THIS PRODUCT: KEEP OUT OF EYES. IN CASE OF CONTACT WITH EYES FLUSH THOROUGHLY WITH WATER.

AVOID CONTACT WITH BROKEN SKIN. DO NOT INHALE OR INGEST. STOP USE AND ASK A DOCTOR IF IRRITATION AND REDNESS APPEARS OR IF CONDITION PERSISTS FOR MORE THEN 72 HOURS.

DOSAGE & ADMINISTRATION SECTION

WET HANDS THOROUGHLY WITH PRODUCT AND ALLOW TO DRY WITHOU WIPING.FOR CHILDRENS UNDER 6 USE ONLY UNDER ADULT SUPERVISION. NOT RECOMMENDED FOR INFANTS.

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.

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL 70 %

INACTIVE INGREDIENT SECTION

AQUA/WATER, ACRYLATES/C 10-30 ALKYL ACRYLATE CROSSPOLYMER, CARBOMER, AMINOMETHYL PROPANOL,ALOE BARBADENSIS LEAF EXTRACT, CI.19140, CI.42090.

OTC - PURPOSE SECTION

TO DECREASE BACTERIA ON THE SKIN THAT COULD CAUSE DISEASE. RECOMMENDE FOR REPEATED USE.

INDICATIONS & USAGE SECTION

WET HANDS THOROUGHLY WITH PRODUCT AND ALLOW TO DRY WITHOU WIPING.

OTC - DO NOT USE SECTION

STOP USE AND ASK A DOCTOR IF IRRITATION AND REDNESS APPERAS OR IF CONDITION PERSISTS FOR MORE THEN 72 HOURS.

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 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73971-30173971-301-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
d64cf554-f776-945c-e053-2a95a90ac172b3db57be-a1f5-711f-e053-2a95a90a3eea2022-01-23WarningsExact identifier
spl set id: b3db57be-a1f5-711f-e053-2a95a90a3eea

Reported adverse events (FAERS/openFDA)#

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