FDA.reportPublic FDA data

Jojo Siwa Hand Sanitizer

Manufacturer
Yozzi Co.,ltd
Effective date
2020-06-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:19:34

Label at a glance#

ProductJojo Siwa Hand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Dosage and administration

​ ​Put a thumbnail size amount in your palm and rub your hands together briskly until dry. Children under 6 years of age should be supervised when using this product. Not recommended for infants.

Storage and handling

• Do not store above 100° F (38 °C). • May discolor some fabrics. • Harmful to wood finishes & plastics.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use:

INDICATIONS & USAGE SECTION

​​To help reduce bacteria and germs on the skin.

WARNINGS:

WARNINGS SECTION

For external use only: hands.

Flammable. Keep away from fire or flame.

When using this product:

• Keep out of eyes. • In case of contact with eyes, flush thoroughly with water. • Avoid contact with broken skin. • Do not inhale or ingest.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

• Keep out of reach of children.

• In case of accidental digestion, seek professional assistance or contact a Poison Control Center immediately.

Directions:

DOSAGE & ADMINISTRATION SECTION

​​Put a thumbnail size amount in your palm and rub your hands together briskly until dry. Children under 6 years of age should be supervised when using this product. Not recommended for infants.

Other Information:

STORAGE AND HANDLING SECTION

• Do not store above 100° F (38 °C).

• May discolor some fabrics.

• Harmful to wood finishes & plastics.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water (Aqua), Glycerin, Propylene Glycol, Carbomer, Triethanolamine, Aloe Barbadensis Leaf Extract, Fragrance, Tocopheryl Acetate (Vitamin E), FD&C Red No. 2, FD&C Blue No. 1

OTC - QUESTIONS SECTION

QUESTIONS OR COMMENTS?

1-877-274-8358 Toll Free in USA

1-909-434-0911 International

SPL UNCLASSIFIED SECTION

KILLS 99% OF MOST COMMON GERMS

©2020 Viacom International Inc. All Rights Reserved. Nickelodeon and all related titles and logos are trademarks of Viacom International Inc. JoJo Siwa is a trademark of JoJo Siwa Entertainment, LLC.

DESIGNED IN U.S.A.

MADE IN CHINA

PATENTS, COPYRIGHTS AND TRADEMARKS GRANTED OR PENDING WORLDWIDE

DISTRIBUTED BY
ASHTEL STUDIOS INC.
ONTARIO, CA 91761

SMARTCAREUS.COM

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN1
581660ethanol 0.62 ML/ML Topical GelSCD1
581660ethanol 62 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72285-006-012022-01-28C16284748780-1d6a99b39-f719-a426-e053-dadaa90af4c2JOJO Siwa Smart Care ® HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72285-006-01Jojo Siwa Hand Sanitizer29 mL in 1 BOTTLEGEL291

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72285-006JOJO SIWA HAND SANITIZER (ETHYL ALCOHOL) GEL [YOZZI CO.,LTD]1Legacy NDC, 1 package rows20200630_fbbe75be-e3d4-4f06-a417-2a592fc70da0.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72285-00672285-006-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
TROLAMINE9O3K93S3TKIACT
ALOE VERA LEAFZY81Z83H0XIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
AMARANTH37RBV3X49KIACT
FD&C BLUE NO. 1H3R47K3TBDIACT

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
0419f288-7d96-436a-8563-051c8df544e6fbbe75be-e3d4-4f06-a417-2a592fc70da02020-06-23WarningsExact identifier
spl id: 0419f288-7d96-436a-8563-051c8df544e6
spl set id: fbbe75be-e3d4-4f06-a417-2a592fc70da0

Reported adverse events (FAERS/openFDA)#

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