FDA.reportPublic FDA data

Minions Hand Sanitizer

Manufacturer
Ashtel Studios, Inc.
Effective date
2019-10-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:01:18

Label at a glance#

ProductMinions 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

DESPICABLE ME 

MINION MADE

KILLS 99% OF GERMS

© Universal City Studios LLC.

QUESTIONS OR COMMENTS?

1-877-274-8358 Toll Free in USA + 1-909-434-0911 International COPYRIGHTS AND TRADEMERKS GRANTED OR PENDING WORLDWIDE

DISTRIBUTED BY ASHTEL STUDIOS INC. ONTARIO, CALIFORNIA 91761

Smart Care®

SMARTCAREUS.COM

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70108-021-012023-07-28C16284748780-10191ceaa-6848-198a-e063-dbdaa90aec3eMinions Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70108-021-01Minions Hand Sanitizer53 mL in 1 BOTTLELIQUID531

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70108-021MINIONS HAND SANITIZER (ETHYL ALCOHOL) LIQUID [ASHTEL STUDIOS, INC.]1Legacy NDC, 1 package rows20191024_050564b2-17a0-4fb3-a61f-3a6a4d5dd74d.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
70108-02170108-021-01

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
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
.ALPHA.-TOCOPHEROLH4N855PNZ1IACT
ALOE VERA LEAFZY81Z83H0XIACT
TROLAMINE9O3K93S3TKIACT
PROPYLENE GLYCOL6DC9Q167V3IACT

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
673dc2b5-4177-43b8-b38a-9e3fd7454886050564b2-17a0-4fb3-a61f-3a6a4d5dd74d2019-10-14WarningsExact identifier
spl id: 673dc2b5-4177-43b8-b38a-9e3fd7454886
spl set id: 050564b2-17a0-4fb3-a61f-3a6a4d5dd74d

Reported adverse events (FAERS/openFDA)#

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