HOLOI

Manufacturer
LIFEN1 LLC
Effective date
2020-06-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:15:43

Label at a glance#

ProductHOLOI
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

Hand Sanitizer to reduce bacteria on the skin, when water and soap are not available. Recommended for repeated use.

Dosage and administration

Spray as much into your pals and thoroughly spread on both hands. Rub into skin until dry. Other information Store at 20 degrees Celsius (66-77 degrees Fahrenheit). May discolor fabrics.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v.

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

Hand Sanitizer to reduce bacteria on the skin, when water and soap are not available. Recommended for repeated use.

Warnings

WARNINGS SECTION

For External Use Only.

Flammable. Keep away from fire or flame.

When using this product, avoid contact with eyes. In case of contact, flush eyes with water. Consult a doctor.

Discontinue use if redness or irritation develop. If condition persist form 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.

Directions

DOSAGE & ADMINISTRATION SECTION

Spray as much into your pals and thoroughly spread on both hands. Rub into skin until dry.

Other information

Store at 20 degrees Celsius (66-77 degrees Fahrenheit).

May discolor fabrics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Vitamin E, Lemon Grass Essential Oil Blend.

Package label principle display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78483-001-01HOLOI30 mL in 1 BOTTLE, PLASTICLIQUID301
78483-001-02HOLOI59 mL in 1 BOTTLE, PLASTICLIQUID591
78483-001-03HOLOI118 mL in 1 BOTTLE, PLASTICLIQUID1181
78483-001-04HOLOI473 mL in 1 BOTTLE, PLASTICLIQUID4731

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78483-001HOLOI (ALCOHOL) LIQUID [LIFEN1 LLC]1Legacy NDC, 4 package rows20200603_75ad61d7-1370-46c7-9018-2f1ec1dfafe1.zip

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
78483-00178483-001-01, 78483-001-02, 78483-001-03, 78483-001-04

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
b1b2cfe4-15e3-4c87-9677-86e9fb4c321375ad61d7-1370-46c7-9018-2f1ec1dfafe12020-06-02WarningsExact identifier
spl id: b1b2cfe4-15e3-4c87-9677-86e9fb4c3213
spl set id: 75ad61d7-1370-46c7-9018-2f1ec1dfafe1

Reported adverse events (FAERS/openFDA)#

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