FDA.reportPublic FDA data

U Instant Hand Sanitizer Aloe Vera

Manufacturer
Zhejiang Shenying Technology Co., Ltd. Jiaojiang Branch
Effective date
2020-08-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:24:50

Label at a glance#

ProductU Instant Hand Sanitizer Aloe Vera
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Place enough product in your palm to thoroughly spread on both hands and rub into skin  untill dry Children under six years of age should be supervised when using this product

Storage and handling

Store below 106F (41C) May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

Flammable. Keep away from fire or flame

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product in your palm to thoroughly spread on both hands and rub into skin  untill dry

Children under six years of age should be supervised when using this product

Other information

STORAGE AND HANDLING SECTION

Store below 106F (41C)

May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, aloe barbadensis leaf jiuce, carbomer, fragrance, glycerin, propylene glycol, triethanolamine, tocopheryl acetate, 2-(dimethylamino) ethanol, FD&C Blue 1, FD&C Yelow 5

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN1
582753ethanol 0.7 ML/ML Topical SolutionSCD1
582753ethanol 70 % Topical SolutionSY1
582753ethyl alcohol 70 % 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
75112-007-012022-01-28C16284748780-1d6a99b39-ad9b-a426-e053-dadaa90af4c210cb80a9-55cf-4c38-8d73-bd011c267bfa
75112-007-022022-01-28C16284748780-1d6a99b39-ad9b-a426-e053-dadaa90af4c210cb80a9-55cf-4c38-8d73-bd011c267bfa
75112-007-032022-01-28C16284748780-1d6a99b39-ad9b-a426-e053-dadaa90af4c210cb80a9-55cf-4c38-8d73-bd011c267bfa
75112-007-042022-01-28C16284748780-1d6a99b39-ad9b-a426-e053-dadaa90af4c210cb80a9-55cf-4c38-8d73-bd011c267bfa
75112-007-052022-01-28C16284748780-1d6a99b39-ad9b-a426-e053-dadaa90af4c210cb80a9-55cf-4c38-8d73-bd011c267bfa
75112-007-062022-01-28C16284748780-1d6a99b39-ad9b-a426-e053-dadaa90af4c210cb80a9-55cf-4c38-8d73-bd011c267bfa
75112-007-072022-01-28C16284748780-1d6a99b39-ad9b-a426-e053-dadaa90af4c210cb80a9-55cf-4c38-8d73-bd011c267bfa
75112-007-082022-01-28C16284748780-1d6a99b39-ad9b-a426-e053-dadaa90af4c210cb80a9-55cf-4c38-8d73-bd011c267bfa
75112-007-092022-01-28C16284748780-1d6a99b39-ad9b-a426-e053-dadaa90af4c210cb80a9-55cf-4c38-8d73-bd011c267bfa

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75112-007-01U Instant Hand Sanitizer Aloe Vera30 mL in 1 BOTTLESOLUTION301
75112-007-02U Instant Hand Sanitizer Aloe Vera54 mL in 1 BOTTLESOLUTION541
75112-007-03U Instant Hand Sanitizer Aloe Vera60 mL in 1 BOTTLESOLUTION601
75112-007-04U Instant Hand Sanitizer Aloe Vera100 mL in 1 BOTTLESOLUTION1001
75112-007-05U Instant Hand Sanitizer Aloe Vera237 mL in 1 BOTTLESOLUTION2371
75112-007-06U Instant Hand Sanitizer Aloe Vera500 mL in 1 BOTTLESOLUTION5001
75112-007-07U Instant Hand Sanitizer Aloe Vera1000 mL in 1 BOTTLESOLUTION10001
75112-007-08U Instant Hand Sanitizer Aloe Vera1800 mL in 1 BOTTLESOLUTION18001
75112-007-09U Instant Hand Sanitizer Aloe Vera3780 mL in 1 BOTTLESOLUTION37801

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75112-007U INSTANT HAND SANITIZER ALOE VERA (ALCOHOL) SOLUTION [ZHEJIANG SHENYING TECHNOLOGY CO., LTD. JIAOJIANG BRANCH]1Legacy NDC, 9 package rows20200817_10cb80a9-55cf-4c38-8d73-bd011c267bfa.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
75112-00775112-007-01, 75112-007-02, 75112-007-03, 75112-007-04, 75112-007-05, 75112-007-06, 75112-007-07, 75112-007-08, 75112-007-09

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
CARBOMER 9404Q93RCW27EIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
TROLAMINE9O3K93S3TKIACT
ALOE VERA LEAFZY81Z83H0XIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
FD&C BLUE NO. 1H3R47K3TBDIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
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
acf660d8-9242-626c-e053-2a95a90ad47710cb80a9-55cf-4c38-8d73-bd011c267bfa2020-08-15WarningsExact identifier
spl id: acf660d8-9242-626c-e053-2a95a90ad477
spl set id: 10cb80a9-55cf-4c38-8d73-bd011c267bfa

Reported adverse events (FAERS/openFDA)#

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