FDA.reportPublic FDA data

Justice Cactus Vanilla Scent Anti-Bacterial Hand Sanitizer

Manufacturer
Tween Brands, Inc.
Effective date
2022-10-07
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:52:01

Label at a glance#

ProductJustice Cactus Vanilla Scent Anti-Bacterial Hand Sanitizer
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping. Supervise children in the use of this product.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

  • For hand washing to decrease bacteria on the skin.
  • Recommended for repeated use.

Warnings

WARNINGS SECTION

Flammable, keep away from fire or flame.

For external use only.

Do not use

OTC - DO NOT USE SECTION

in the eyes or apply over large areas of the body.

In case of deep or puncture wounds, animal bites or serious burns, consult a doctor.

Use only as directed. Do not drink. If taken Internally, It will produce serious gastric disturbances.

Stop use and ask a doctor If

OTC - STOP USE SECTION

Irritation persists for more than 72 hours.

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

  • Wet hands thoroughly with product and allow to dry without wiping.
  • Supervise children in the use of this product.

Other information

SPL UNCLASSIFIED SECTION

  • Store below 105°F(40.5°C).
  • May discolor some fabrics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Propylene Glycol, Fragrance, Carbomer, Triethanolamie, D&C Red No. 33.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label1Label1

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60637-06160637-061-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CARBOXYPOLYMETHYLENE0A5MM307FCIACT
TROLAMINE9O3K93S3TKIACT
D&C RED NO. 339DBA0SBB0LIACT
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
ed34a158-b0e0-5410-e053-2995a90a87537dbba25e-1dcf-46e4-91dc-ea8de3d7ebd02022-11-11WarningsExact identifier
spl set id: 7dbba25e-1dcf-46e4-91dc-ea8de3d7ebd0

Reported adverse events (FAERS/openFDA)#

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