FDA.reportPublic FDA data

Ili Hand Sanitizer

Manufacturer
Strong Brands, Inc.
Effective date
2010-06-30
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 22:25:47

Label at a glance#

ProductIli Hand Sanitizer Instant
Active ingredientAlcohol
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Ethyl Alcohol 63%

OTC - PURPOSE SECTION

Purpose: Antiseptic

INDICATIONS & USAGE SECTION

Use: For hand washing to decrease bacteria on the skin. Recommended for repeated use.

WARNINGS SECTION

Warnings: Flammable, keep away from fire or flame. For external use only. Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develop. If condition persists for more than 72 hours consult a doctor.

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.

DOSAGE & ADMINISTRATION SECTION

Directions: Wet hands thoroughly with product and allow to dry without wiping.

OTC - QUESTIONS SECTION

Questions? 1-323-284-9021 weekdays, 9am to 5pm PST

ili Hand Sanitizer 8 fl oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

8 fl oz Ili Hand Sanitizer Label8 fl oz Ili Hand Sanitizer LabelMM1:8floz_ILI_Hand_Sanitizer_Label rev 3_Page_1.jpg

INACTIVE INGREDIENT SECTION

water, isopropyl alcohol, glycerin, methyl gluceth-20, panthenol, tocopheryl acetate, benzalkonium chloride, polysorbate 20, carbomer, sodium benzotriazolyl butylphenol sulfonate, aminomethyl propanol, fragrance

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1094724ethanol 63 % Topical GelPSN3
1094724ethanol 0.63 ML/ML Topical GelSCD3
1094724ethanol 63 % Topical GelSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50859-100-012019-10-21C16284748780-1956f9ecf-d2e7-621f-e053-dbdaa90a74adDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50859-100-01Ili Hand SanitizerInstant236.6 mL in 1 BOTTLE, PUMPGEL236.63

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50859-100ILI HAND SANITIZER INSTANT (ALCOHOL) GEL [STRONG BRANDS, INC.]3Legacy NDC, 1 package rows20100911_760828bc-3e08-493e-b3e4-efc5dba98a34.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AlcoholACTIVE INGREDIENT3K9958V90M3
AlcoholACTIVE MOIETY3K9958V90M3

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50859-10050859-100-01

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
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
5dc4d6ba-525d-412b-9bc9-8bd17595b3bb760828bc-3e08-493e-b3e4-efc5dba98a342010-06-30WarningsExact identifier
spl id: 5dc4d6ba-525d-412b-9bc9-8bd17595b3bb
spl set id: 760828bc-3e08-493e-b3e4-efc5dba98a34

Reported adverse events (FAERS/openFDA)#

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