FDA.reportPublic FDA data

aurafresh instant hand sanitizer

Manufacturer
Ningbo Pulisi Daily Chemical Products Co., Ltd.
Effective date
2017-08-11
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 22:52:11

Label at a glance#

Productaurafresh instant hand sanitizer aloe vera
Active ingredientalcohol
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient                                  Purpose

Ethyl Alcohol                70%      ...        Antiseptic

OTC - PURPOSE SECTION

Hand sanitizer to help decrease bacteria on the skin.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact local poison control center right away.

Children under 6 years of age should be supervised when using this products.

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

For external use only.
Flammable. Keep away from hear or flame.

Stop using and ask a doctor, if irritation or rash appears and lasts.

DOSAGE & ADMINISTRATION SECTION

place enough product in your palm and thoroughly spread on both hands, and rub into the skin until dry.

other information: store below 106 Degrees Fahrenheit (41 Degrees Centigrade); may discolor certain fabrics or surface.

INACTIVE INGREDIENT SECTION

Water, Carbomer, Glycerin, Propylene Glycol, acrylates/c10-30 alkyl acrylate crosspolymer, isopropyl alcohol, aminoethyl propanol, isopropyl myristate, caprylyl glycol, phenoxyenthanol, Triethanolamine, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Fragrance, blue 1, yellow 5

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of labelimage of label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN4
581662ethanol 0.7 ML/ML Topical GelSCD4
581662ethanol 70 % Topical GelSY4
581662ethyl alcohol 70 % Topical GelSY4

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130636160141965GTIN-13: 0636160141965
EAN-13: 0636160141965
GTIN-12: 636160141965
UPC-A: 636160141965
GTIN storage (14 digits): 00636160141965		aurafresh hand sanitizer(aloe vera) 2 (2x2)oz.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
40104-283-012020-01-31C16284748780-19d75b9cf-dbcb-f424-e053-dadaa90a57ceDrug facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
40104-283-01aurafresh instant hand sanitizeraloe vera60 mL in 1 BOTTLEGEL604
40104-283-01aurafresh instant hand sanitizeraloe vera2 in 1 PACKAGEGEL24

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
40104-283AURAFRESH INSTANT HAND SANITIZER ALOE VERA (ALCOHOL) GEL [NINGBO PULISI DAILY CHEMICAL PRODUCTS CO., LTD.]4Legacy NDC, 2 package rows20170811_93ab252c-0541-4cd5-a823-21e908016686.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
40104-28340104-283-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
alcohol3K9958V90MACTIB
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ALOE VERA LEAFZY81Z83H0XIACT
CARBOMER 934Z135WT9208IACT
GLYCERINPDC6A3C0OXIACT
.ALPHA.-TOCOPHEROL ACETATE, D-A7E6112E4NIACT
TROLAMINE9O3K93S3TKIACT
CARBOMER COPOLYMER TYPE A71DD5V995LIACT
ISOPROPYL ALCOHOLND2M416302IACT
AMINOMETHYLPROPANOLLU49E6626QIACT
CAPRYLYL GLYCOL00YIU5438UIACT
PHENOXYETHANOLHIE492ZZ3TIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
FD&C YELLOW NO. 5I753WB2F1MIACT

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
805919bf-734b-476c-af2c-546ceee69fdb93ab252c-0541-4cd5-a823-21e9080166862017-08-11WarningsExact identifier
spl id: 805919bf-734b-476c-af2c-546ceee69fdb
spl set id: 93ab252c-0541-4cd5-a823-21e908016686

Reported adverse events (FAERS/openFDA)#

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