FDA.reportPublic FDA data

Jack N Jill Dino Hand Sanitizer

Manufacturer
Jack & Jill Operations Pty Ltd
Effective date
2023-12-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:18:25

Label at a glance#

ProductJack N Jill Dino Hand Sanitizer
Active ingredientALCOHOL
Label structure6 sections

Indications and uses

To help reduce bacteria on the skin

Dosage and administration

squeeze a pea sized drop onto the palm of one hand and rub hands together, distribute over all surfaces of hands and fingers until dry.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol (62%)

Purpose

OTC - PURPOSE SECTION

Anti-bacterial 

Uses

INDICATIONS & USAGE SECTION

  • To help reduce bacteria on the skin

Warnings

WARNINGS SECTION

Flammable - keep away from fire or flame.

For external use only.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or redness develops.

Children under 6 years of age should be supervised when using this product. Not recommended for infants.

In case of eye contact, flush eyes with water. Avoid contact with eyes.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • squeeze a pea sized drop onto the palm of one hand and rub hands together, distribute over all surfaces of hands and fingers until dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION

aminomethyl propanol, carbomer, glycerin, propylene glycol, water

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle4Bottle4

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78161-00778161-007-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
AMINOMETHYLPROPANOLLU49E6626QIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
WATER059QF0KO0RIACT
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
1cc13e6b-f751-5da0-e063-6294a90a43fbf8647497-d366-4135-8048-a1cd2332f2ba2024-07-08WarningsExact identifier
spl set id: f8647497-d366-4135-8048-a1cd2332f2ba

Reported adverse events (FAERS/openFDA)#

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