Fiori Gallon HandSanitizer

Manufacturer
International Merchandise Group | Distribuidora Cuscatlan
Effective date
2020-11-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:05:55

Label at a glance#

ProductFiori Gallon HandSanitizer
Active ingredientALCOHOL
Label structure9 sections

Label contents#

Full prescribing information#

WARNINGS SECTION

DO NOT SORE ABOVE 105 F MAY DISCOLOR SOME FABRICS. HARMFULA TO WOOD FINISHES AND PLASTICS. FOR HANDS ESTERNAL 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 REDNESS OR IF CONDITION PERSISTS FOR MORE THEN 72 HOURS.

DOSAGE & ADMINISTRATION SECTION

WET HAND THOROUGHLY WITH PRODUCT AND ALLOW TO DRY WITHOU WIPING FOR CHILDREN UNDER 6 USE ONLY UNDER ADULT SUPERVISION.NOT RECOMENDED 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/C10-30 ALKYLL ACRYLATE CROSSPOLYMER, CARBOMER AMINOMETHYL PROPANOL

OTC - PURPOSE SECTION

TO DECREASE BACTERIAS ON THE SKIN THAT COULD CAUSE DISEAASE, RECOMENDED FOR REPEATED USE.

INDICATIONS & USAGE SECTION

FOR HANDS EXTERNAL USE ONLY

OTC - DO NOT USE SECTION

DO NOT INHALE OR INGEST.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

front back Gallonfront back Gallon

Products#

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73971-30273971-302-04

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
d64d0373-59ac-6b59-e053-2995a90a0ff6b4c024ef-1dfa-41f1-e053-2995a90a46252022-01-23WarningsExact identifier
spl set id: b4c024ef-1dfa-41f1-e053-2995a90a4625

Reported adverse events (FAERS/openFDA)#

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