FDA.reportPublic FDA data

Kimtrue Instant Hand Sanitizer

Manufacturer
Velocity Beauty Group LLC
Effective date
2020-12-29
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:59:35

Label at a glance#

ProductKimtrue Instant Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Storage and handling

Other information do not store above 104°F (40°C).

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Ethyl Alcohol 70% v/v

OTC - PURPOSE SECTION

Purpose

Antiseptic

WARNINGS SECTION

For external use only. Flammable. Keep away from fire or flame.

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. If eye contact occurs, rinse with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if skin irritation or redness develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingestion, seek medical help or contact a Poison Control Center immediately.

INDICATIONS & USAGE SECTION

Uses to help reduce bacteria on the skin

DOSAGE & ADMINISTRATION SECTION

Directions apply enough gel to wet hands and rub together until dry. Use 1 to 3 times daily.

STORAGE AND HANDLING SECTION

Other information do not store above 104°F (40°C).

INACTIVE INGREDIENT SECTION

Inactive ingredients Aloe Barbadensis Leaf Juice, Carthamus Tinctorius (Safflower) Oleosomes*, Cympobogon Flexuosus (Lemongrass Oil, Fragrance (Parfum), Glycerin, Hydroxyethylcellulose, Helianthus Annuus (Sunflower) Seed Oil, , Lonicera Caprifolium (Honeysuckle) Flower Extract, Lonicera Japonica (Honeysuckle) Flower Extract, PEG-40 Hydrogenated Castor Oil, Rosmarinus Officinalis (Rosemary) Leaf Extract, Sodium Hyaluronate, Water (Aqua). May contain Isopropyl Alcohol.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

KTIHS16KTIHS16

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78686-07078686-070-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%)R33S7TK2EPIACT
CARTHAMUS TINCTORIUS SEED OLEOSOMES9S60Q72309IACT
ALOE VERA LEAFZY81Z83H0XIACT
ISOPROPYL ALCOHOLND2M416302IACT
GLYCERINPDC6A3C0OXIACT
SUNFLOWER OIL3W1JG795YIIACT
ROSEMARYIJ67X351P9IACT
LONICERA JAPONICA FLOWER4465L2WS4YIACT
ALCOHOL3K9958V90MACTIB
PEG-40 CASTOR OIL4ERD2076EFIACT
CYMBOPOGON FLEXUOSUS LEAF7LJ4Y1UJG7IACT
WATER059QF0KO0RIACT
HYALURONATE SODIUMYSE9PPT4THIACT
LONICERA CAPRIFOLIUM FLOWER5N1WD9784UIACT

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
b794447c-95ae-7851-e053-2995a90ac66aa863cb86-f449-243e-e053-2995a90ab8352020-12-29WarningsExact identifier
spl id: b794447c-95ae-7851-e053-2995a90ac66a
spl set id: a863cb86-f449-243e-e053-2995a90ab835

Reported adverse events (FAERS/openFDA)#

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