FDA.reportPublic FDA data

Jack N Jill Bunny 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 21:18:17

Label at a glance#

ProductJack N Jill Bunny Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
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

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • To help reduce bacteria on the skin

Warnings

WARNINGS SECTION

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

Hydroxyethylcellulose, Phenoxyethanol, Water

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

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
78161-00478161-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
HYDROXYETHYL CELLULOSE, UNSPECIFIEDT4V6TWG28DIACT
PHENOXYETHANOLHIE492ZZ3TIACT
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
1cc14689-54f3-34ee-e063-6394a90a77175bb2a29d-46ca-45eb-9787-6174c5a12cc42024-07-08WarningsExact identifier
spl set id: 5bb2a29d-46ca-45eb-9787-6174c5a12cc4

Reported adverse events (FAERS/openFDA)#

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