Paw Patrol Hand Sanitizer

Manufacturer
Ashtel Studios, Inc.
Effective date
2019-07-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:59:57

Label at a glance#

ProductPaw Patrol Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

Use To help reduce bacteria and germs on the skin.

WARNINGS SECTION

WARNING Flammable. Keep away from fire or flame. For external use only • Stop use and ask a doctor if irritation or redness develops and persists.

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.

DOSAGE & ADMINISTRATION SECTION

Directions • Place enough product in palm to cover hands and rub hands together briskly until dry. • Children under 6, use only under adult supervision. • Not recommended for infants.

STORAGE AND HANDLING SECTION

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

INACTIVE INGREDIENT SECTION

Inactive Ingredients • Deionized Water, Glycerine, Carbomer, Vitamin E, Fragrance, Aloe Barbadensis Gel, Triethanolamine, Propylene Glycol.

SPL UNCLASSIFIED SECTION

KILLS 99% OF GERMS

Smart Care®

© 2019 Spin Master PAW Productions Inc. All Rights Reserved. PAW Patrol and all related titles, logos and characters are trademarks of Spin Master Ltd. Nickelodeon and all related titles and logos are trademarks of Viacom International Inc.

QUESTIONS OR COMMENTS?

1-877-274-8358 Toll Free in USA • 1-909-434-0911 International COPYRIGHTS AND TRADEMARKS GRANTED OR PENDING WORLDWIDE SMARTCAREUS.COM • ONTARIO, CA  ITEM#: 70229-24

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
247835ethanol 62 % Topical SolutionPSN1
247835ethanol 0.62 ML/ML Topical SolutionSCD1
247835ethanol 62 % Topical SolutionSY1
247835ethyl alcohol 62 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70108-018-012023-07-28C16284748780-10191ceaa-7002-198a-e063-dbdaa90aec3ePaw Patrol Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70108-018-01Paw Patrol Hand Sanitizer53 mL in 1 BOTTLELIQUID531

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70108-018PAW PATROL HAND SANITIZER (ETHYL ALCOHOL) LIQUID [ASHTEL STUDIOS, INC.]1Legacy NDC, 1 package rows20190731_716b1807-61a2-4fc5-9590-014044a20085.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70108-01870108-018-01

Ingredients#

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

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

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
67f27bff-a371-4c2d-a661-3e4d9337f5a7716b1807-61a2-4fc5-9590-014044a200852019-07-24WarningsExact identifier
spl id: 67f27bff-a371-4c2d-a661-3e4d9337f5a7
spl set id: 716b1807-61a2-4fc5-9590-014044a20085

Reported adverse events (FAERS/openFDA)#

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