FDA.reportPublic FDA data

aurafresh instant hand sanitizer with moisturizeers

Manufacturer
Ningbo Pulisi Daily Chemical Products Co., Ltd.
Effective date
2017-08-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:52:11

Label at a glance#

Productaurafresh instant hand sanitizer with moisturizeers vitamin E and aloe
Active ingredientalcohol
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient                                  Purpose

Ethyl Alcohol                62%      ...        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 must be supervised in use of this product.

INDICATIONS & USAGE SECTION

keep out of eyes

when water, soap and towel are not available

WARNINGS SECTION

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

Do not apply around eyes; Do not use in ears and mouth. When using this products, avoid contact with eyes. In case of contact, flush eyes with water.

Stop using and ask a doctor, if irritation and redness develops, if condition persists for more than 72 hours, consult a doctor.

DOSAGE & ADMINISTRATION SECTION

Pump as needed into your palms and thoroughly spread on both hands, and rub the skin until dry.

INACTIVE INGREDIENT SECTION

Water, Carbomer, Glycerin, Propylene Glycol, Triethanolamine, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of labelimage of label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN1
581660ethanol 0.62 ML/ML Topical GelSCD1
581660ethanol 62 % Topical GelSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130636160141934GTIN-13: 0636160141934
EAN-13: 0636160141934
GTIN-12: 636160141934
UPC-A: 636160141934
GTIN storage (14 digits): 00636160141934		aurafresh hand sanitizer(vitamin E and aloe ) 8 oz.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
40104-281-012020-01-31C16284748780-19d75b9d0-3250-f424-e053-dadaa90a57ceDrug facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
40104-281-01aurafresh instant hand sanitizer with moisturizeersvitamin E and aloe237 mL in 1 BOTTLEGEL2371

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
40104-281AURAFRESH INSTANT HAND SANITIZER WITH MOISTURIZEERS VITAMIN E AND ALOE (ALCOHOL) GEL [NINGBO PULISI DAILY CHEMICAL PRODUCTS CO., LTD.]1Legacy NDC, 1 package rows20170810_a887c1f6-adae-4e63-b523-fc55317a204d.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
40104-28140104-281-01

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
PROPYLENE GLYCOL6DC9Q167V3IACT
ALOE VERA LEAFZY81Z83H0XIACT
CARBOMER 934Z135WT9208IACT
GLYCERINPDC6A3C0OXIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
TROLAMINE9O3K93S3TKIACT

Source Document#

Source XML · Source PDF

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
5bb95936-f42b-4458-8e67-91dac5906bb7a887c1f6-adae-4e63-b523-fc55317a204d2017-08-10WarningsExact identifier
spl id: 5bb95936-f42b-4458-8e67-91dac5906bb7
spl set id: a887c1f6-adae-4e63-b523-fc55317a204d

Reported adverse events (FAERS/openFDA)#

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