FDA.reportPublic FDA data

Instukem Hand Sanitizer Moisturizing Gel

Manufacturer
Services Instukem Ltée
Effective date
2020-11-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:05:13

Label at a glance#

ProductInstukem Hand Sanitizer Moisturizing
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

• Place enough product on hands to cover all surfaces. Rub hands together until dry. • Supervise children under 6 of age when using this product to avoid swallowing.

Storage and handling

• Store between 15-30ºC (59-86ºF) • Avoid freezing and excessive heat above 40ºC (104ºF)

Label contents#

Full prescribing information#

ACTIVE INGREDIENT(S)

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70% v/v

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

USE(S)

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

WARNINGS

WARNINGS SECTION

For external use only. Keep away from heat or flame.

Do not use:

OTC - DO NOT USE SECTION

• on children less than 2 months of age
• on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop using this product and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a poison Control Center right away.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 of age when using this product to avoid swallowing.

OTHER INFORMATION

STORAGE AND HANDLING SECTION

• Store between 15-30ºC (59-86ºF)
• Avoid freezing and excessive heat above 40ºC (104ºF)

INACTIVE INGREDIENT(S)

INACTIVE INGREDIENT SECTION

Water, glycerin, acrylates/C10-30 alkyl acrylate crosspolymer, triethanolamine

Package Labelling: 77984-007-00

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

bottlebottle

Package Labelling: 77984-007-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package Labelling image descriptionimage description

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
77984-00777984-007-00, 77984-007-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
TROLAMINE9O3K93S3TKIACT
ALCOHOL3K9958V90MACTIB
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT

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
efd07a07-15a0-85f9-e053-2995a90af471b5591dd3-5d95-17db-e053-2995a90a19852022-12-14WarningsExact identifier
spl set id: b5591dd3-5d95-17db-e053-2995a90a1985

Reported adverse events (FAERS/openFDA)#

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