FDA.reportPublic FDA data

XtraCare Hand Sanitizer Antibacterial Moisturize with Vitamin E

Manufacturer
Rejoice Industries Canada Inc.
Effective date
2026-04-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:57:34

Label at a glance#

ProductXtraCare Hand Sanitizer Antibacterial Moisturize with Vitamin E
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

for handwashing to decrease bacteria on the skin recommended for repeated use

Dosage and administration

wet hands thoroughly with product. briskly rub hands together until dry supervise children under 6 years in the use of this product

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70.0% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • for handwashing to decrease bacteria on the skin
  • recommended for repeated use

Warnings

WARNINGS SECTION

For external use only.

Flammable, keep away from heat and flame.

Do not use

OTC - DO NOT USE SECTION

in the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation and redness develop and persist 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.
  • briskly rub hands together until dry
  • supervise children under 6 years in the use of this product

Other information

SPL UNCLASSIFIED SECTION

  • store at room temperature
  • may discolor certain fabrics

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, carbomer, glycerin, propylene glycol, aminomethyl propanol, fragrance, aloe barbadensis leaf juice, tocopheryl acetate.

Questions/comments?

OTC - QUESTIONS SECTION

1-855-345-5575

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130639277922069GTIN-13: 0639277922069
EAN-13: 0639277922069
GTIN-12: 639277922069
UPC-A: 639277922069
GTIN storage (14 digits): 00639277922069		Label2.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87559-000-01XtraCare Hand Sanitizer Antibacterial Moisturize with Vitamin E236 mL in 1 BOTTLE, PLASTICGEL2361
87559-000-01XtraCare Hand Sanitizer Antibacterial Moisturize with Vitamin E1 in 1 CARTONGEL11

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87559-00087559-000-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
AMINOMETHYLPROPANOLLU49E6626QIACT
ALOE VERA LEAF JUICERUE8E6T4NBIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
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
XtraCare Hand Sanitizer Antibacterial Moisturize with Vitamin EALCOHOLRejoice Industries Canada Inc.b79d4c90-6e5c-475f-9bb3-6017a2d637932026-04-07WarningsExact identifier
ndc (package): 87559-000-01
ndc (product): 87559-000
ndc11 (package): 87559000001
spl id: 4ee1f6a3-0a4c-f258-e063-6294a90a81f3
spl set id: b79d4c90-6e5c-475f-9bb3-6017a2d63793

Reported adverse events (FAERS/openFDA)#

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