FDA.reportPublic FDA data

NexSense Liquid Hand Sanitizer Moisturizing with Aloe

Manufacturer
Taizhou Yadai Daily-Use Co., Ltd.
Effective date
2020-06-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:18:21

Label at a glance#

ProductNexSense Liquid Hand Sanitizer Moisturizing with Aloe
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

Pump as needed into your palms and thoroughly spead on both hands rub into skin until dry

Storage and handling

Store at room temperature no higher than 45C (115F) and under shade Keep in closed containers and free from direct sunlight 

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help decrease bacteria on the skin

Recommended for repeated use

Warnings

WARNINGS SECTION

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

Do not apply around eyes or use in ears or mouth

Stop use and contact a doctor if redness or irritation develop or persist for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Pump as needed into your palms and thoroughly spead on both hands
  • rub into skin until dry

Other information

STORAGE AND HANDLING SECTION

  • Store at room temperature no higher than 45C (115F) and under shade
  • Keep in closed containers and free from direct sunlight 

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerol, Aminomethyl propanol, Aloe Vera gel, Vitamin E, Carbomer, Frangrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

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
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52989-003-012021-07-23C16284748780-1c7ccaba7-2670-fd44-e053-dadaa90aa01b52989-003
52989-003-022021-07-23C16284748780-1c7ccaba7-2670-fd44-e053-dadaa90aa01b52989-003
52989-003-032021-07-23C16284748780-1c7ccaba7-2670-fd44-e053-dadaa90aa01b52989-003

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52989-003-01NexSense Liquid Hand Sanitizer Moisturizing with Aloe60 mL in 1 BOTTLESOLUTION601
52989-003-02NexSense Liquid Hand Sanitizer Moisturizing with Aloe250 mL in 1 BOTTLESOLUTION2501
52989-003-03NexSense Liquid Hand Sanitizer Moisturizing with Aloe500 mL in 1 BOTTLESOLUTION5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52989-003NEXSENSE LIQUID HAND SANITIZER MOISTURIZING WITH ALOE (ALCOHOL) SOLUTION [TAIZHOU YADAI DAILY-USE CO., LTD.]1Legacy NDC, 3 package rows20200620_0481b42e-d238-4bce-a3cc-02cf1f45107b.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52989-00352989-003-01, 52989-003-02, 52989-003-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
CARBOMER 934Z135WT9208IACT
TROLAMINE9O3K93S3TKIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
ALOE VERA WHOLEKIZ4X2EHYXIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
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
a871c5c9-a704-5634-e053-2995a90a34670481b42e-d238-4bce-a3cc-02cf1f45107b2020-06-19WarningsExact identifier
spl id: a871c5c9-a704-5634-e053-2995a90a3467
spl set id: 0481b42e-d238-4bce-a3cc-02cf1f45107b

Reported adverse events (FAERS/openFDA)#

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