FDA.reportPublic FDA data

Hand Sanitizer Motion PLUS

Manufacturer
M & J Sunshine, Corp.
Effective date
2020-06-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:18:02

Label at a glance#

ProductHand Sanitizer Motion PLUS
Active ingredientALCOHOL
Label structure9 sections

Storage and handling

Other information  • Store below 110°F (43°C). • May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Ethyl alcohol 80% 

OTC - PURPOSE SECTION

Purpose

Antiseptic

INDICATIONS & USAGE SECTION

Uses • This product can be used as a hand and spray sanitizer for use on hands. • Use it to clean any type of surface that virus can live  on a

prolonged period of time

WARNINGS SECTION

Warnings

Flammable.

Keep away from fire or flame/ For external use only.

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash appears and lasts. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions • Put enough product in your palm to cover hands and rub hands together briskly until dry. Children under 6 years of age

should be supervised when using Motion-Plus• Hand Sanitizer.

STORAGE AND HANDLING SECTION

Other information • Store below 110°F (43°C). • May discolor certain fabrics or surfaces.

INACTIVE INGREDIENT SECTION

Inactive ingredients Water(Aqua), Isopropyl Alcohol, Caprylyl Glycol, Glycerin, Isopropyl Myristate, Tocopheryl Acetate,

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol.

SPL UNCLASSIFIED SECTION

DESINFECTANTE DE MANOS

FORMULATED FOR TOP PERFORMANCE

FDA APPROVED Quality

FDA APPROVED TO FIGHT OFF THE COVID-19

ALONG WITH OTHER GERMS AND BACTERIA'S

FDA Approved and Regulated

Worldwide Represented by:

M & J SUNSHINE, CORP.

MIAMI, FL 33166 / FAX: (305) 888 1157

MADE IN USA

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

untitleduntitled

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039339ethanol 80 % Topical SolutionPSN1
1039339ethanol 0.8 ML/ML Topical SolutionSCD1
1039339ethanol 80 % Topical SolutionSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77783-001-032022-01-28C16284748780-1d6a99b39-dbd0-a426-e053-dadaa90af4c2MOTiOn PLUS TM Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77783-001-03Hand Sanitizer Motion PLUS3785 mL in 1 BOTTLELIQUID37851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77783-001HAND SANITIZER MOTION PLUS (ETHYL ALCOHOL) LIQUID [M & J SUNSHINE, CORP.]1Legacy NDC, 1 package rows20200618_3fd72501-bb88-41a0-8e47-b14050b5b4a8.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77783-00177783-001-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302IACT
CAPRYLYL GLYCOL00YIU5438UIACT
GLYCERINPDC6A3C0OXIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
AMINOMETHYLPROPANOLLU49E6626QIACT

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
1ce747ec-bc14-4fbb-8e99-c5d86d0848ad3fd72501-bb88-41a0-8e47-b14050b5b4a82020-06-10WarningsExact identifier
spl id: 1ce747ec-bc14-4fbb-8e99-c5d86d0848ad
spl set id: 3fd72501-bb88-41a0-8e47-b14050b5b4a8

Reported adverse events (FAERS/openFDA)#

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