Fiori Aloe Vera Hand Sanitizer

Manufacturer
International Merchandise Group | distribuidora Custcatlan
Effective date
2020-07-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:21:25

Label at a glance#

ProductFiori Aloe Vera Hand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Dosage and administration

To decrease bacterias on the skin that could disease. Recomended for repeated used.

Label contents#

Full prescribing information#

Warnings

WARNINGS SECTION

Do Not Store above 105 F May discolor some Fabrics. Harmful to wood Finishes and Plastics

For External Use 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 rednes appears or if condition persist for more then 72 hours.

Keep out of reach of Children.

If Swallowed, get medical help or contact a poison control center right away.

For Hands external use only

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aqua/Water,Acrylates/ C 10-30 ALKYL ACRYLATE CROSSPOLYMER, CARBOMER, AMINOMETHYL PROPANOL, ALOE BARBADENSIS LEAF EXTRACT, CI 19140,CI,42090

Directions

INTENDED USE OF THE DEVICE

To decrease bacterias on the skin that could disease. Recomended for repeated used.

keep Out of Reach of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep Out of Reach of Children

ALCOHOL

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL 70 %

Dosage & administration section

ROUTE, METHOD AND FREQUENCY OF ADMINISTRATION

For Topical use only Fpr Hands EXTERNAL USE ONLY

Indications & usage section

To decrease bacterias on the skin that could cause disease.

Purpose section

OTC - PURPOSE SECTION

Hand Sanitizer

Dosage & administration section

For Topical use only

BACK LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BACK LABELBACK LABELFRONT LABELFRONT LABEL

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73971-19073971-190-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
aa69def0-ec70-2b4d-e053-2a95a90a0374aa5d940f-3b3f-de10-e053-2995a90a7e242020-07-14WarningsExact identifier
spl id: aa69def0-ec70-2b4d-e053-2a95a90a0374
spl set id: aa5d940f-3b3f-de10-e053-2995a90a7e24

Reported adverse events (FAERS/openFDA)#

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