FDA.reportPublic FDA data

Instant Hand Sanitizer

Manufacturer
Acessory Myxx LLC | Nantong Health & Beyond Hygienic Products Inc. | NINGBO OCEANSTAR CHEMICAL PRODUCTS CO LTD
Effective date
2020-04-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:06:43

Label at a glance#

ProductInstant Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Label contents#

Full prescribing information#

Instant Hand Sanitizer

WARNINGS SECTION

Warnings
For external use only: hands

Keep out of reach of
children.If swallowed, get
medical help or contact a
Poison Control Center right
away.

Stop use and ask a doctor
if irritation and redness
develop condition persists
for more than 72 hours

aviid contact with broken
skin do not inhale or
ingest

General Warnings

GENERAL PRECAUTIONS SECTION

Warnings
For external use only: hands

Keep out of reach of
children.If swallowed, get
medical help or contact a
Poison Control Center right
away.

Stop use and ask a doctor
if irritation and redness
develop condition persists
for more than 72 hours

aviid contact with broken
skin do not inhale or
ingest

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 62%

INDICATIONS & USAGE SECTION

Use to decrease bacteria on the skin. Use on hands only.

INACTIVE INGREDIENT SECTION

Water, Aloe Barbadensis Leaf Juice,
Maltodextrin,Glycerin, Propylene
Glycol, Acrylates/C10-30 Alkyl
Acrylate Crosspolymer,
Triethanoamine, Fragrance, Lactose,
Microcrystalline Cellulose,Sucrose,
Zea Mays(Corn) starch, Ultramarine
blue CI 77007,Tocopheryl Acetate,
Hydroxypropyl Methyl Cellulose,
D&C Red NO.33, FD&C Blue No.1

OTC - PURPOSE SECTION

To clean hands and fight bacteria on that skin

DOSAGE & ADMINISTRATION SECTION

Squeeze the bottle on your hands so the liquid comes out. Rub hands together. Allow hands to dry.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Not intended for children under the age of 12. Please keep out of reach of children.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DisplayDisplayLabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN2
581660ethanol 0.62 ML/ML Topical GelSCD2
581660ethanol 62 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72619-1001-12024-01-30C16284748780-19d75b9d1-1365-f424-e053-dadaa90a57ceHand Sanitizer
72619-1219-12024-01-30C16284748780-19d75b9d1-1365-f424-e053-dadaa90a57ceHand Sanitizer
72619-1001-12022-01-28C16284748780-19d75b9d1-1365-f424-e053-dadaa90a57ceHand Sanitizer
72619-1219-12022-01-28C16284748780-19d75b9d1-1365-f424-e053-dadaa90a57ceHand Sanitizer
72619-1219-12020-04-17C16284748780-19d75b9d1-1365-f424-e053-dadaa90a57ceHand Sanitizer
72619-1219-12020-01-31C16284748780-19d75b9d1-1365-f424-e053-dadaa90a57ceHand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72619-1001-1Instant Hand Sanitizer2.9 mL in 1 BOTTLE, PLASTICGEL2.92
72619-1219-1Instant Hand Sanitizer2.9 mL in 1 BOTTLE, PLASTICGEL2.92

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72619-1001INSTANT HAND SANITIZER GEL [ACESSORY MYXX LLC]2Legacy NDC, 1 package rows20200418_75d8492a-8e5a-4a6d-e053-2991aa0ad56f.zip
72619-1219INSTANT HAND SANITIZER GEL [ACESSORY MYXX LLC]2Legacy NDC, 1 package rows20200418_75d8492a-8e5a-4a6d-e053-2991aa0ad56f.zip

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72619-121972619-1219-1
72619-100172619-1001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
MICROCRYSTALLINE CELLULOSEOP1R32D61UIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
LACTOSE MONOHYDRATEEWQ57Q8I5XIACT
SUCROSEC151H8M554IACT
ZEA MAYS POLLEN74PD8J616HIACT
ULTRAMARINE BLUEI39WR998BIIACT
3-HEXYLOXYPROPYLENE GLYCOL3485P35DA4IACT
(C10-C30)ALKYL METHACRYLATE ESTERXH2FQZ38D8IACT
GLYCERINPDC6A3C0OXIACT
MALTODEXTRIN7CVR7L4A2DIACT
D&C RED NO. 339DBA0SBB0LIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
CARBOMER 9404Q93RCW27EIACT
TROLAMINE9O3K93S3TKIACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
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
a3329f01-b33f-f733-e053-2995a90a2c7375d8492a-8e5a-4a6d-e053-2991aa0ad56f2020-04-13WarningsExact identifier
spl id: a3329f01-b33f-f733-e053-2995a90a2c73
spl set id: 75d8492a-8e5a-4a6d-e053-2991aa0ad56f

Reported adverse events (FAERS/openFDA)#

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