FDA.reportPublic FDA data

Hand Sanitizer with Aloe

Manufacturer
Target Corporation | Fujian Haojin Toiletries Co Ltd.
Effective date
2020-12-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:35:36

Label at a glance#

ProductHand Sanitizer with Aloe
Active ingredientALCOHOL
Label structure14 sections

Dosage and administration

Apply a dime size amount to hands. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

  • Hand snitizer to help reduce bacteria that potentially can cause disease.
  • For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only.

Flammable, Keep away from fire and flame

Do not use

OTC - DO NOT USE SECTION

  • On childern less than 2 months of age.
  • On open skin wounds.

When using this product

OTC - WHEN USING SECTION

  • Keep out of eyes, ears, and mouth. In case of conatct with eyes, rinse thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develops and persists.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, conatct a doctor or Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply a dime size amount to hands. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

SPL UNCLASSIFIED SECTION

Store between 59-86°F. Avoid freezing and excessive heat above 104°F.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water/Aqua/Eau, Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, T-Butyl Alcohol, Aminomethyl Propanol, Aloe Barbadensis Leaf Extract, Tocopheryl Acetate, Denatonium Benzoate, FD&C Yellow No.5 (CI 19140), FD&C Blue No.1 (CI 42090).

Questions?

OTC - QUESTIONS SECTION

Call 1-800-910-6874

Distributed By

SPL UNCLASSIFIED SECTION

Target Corporation

Minneapolis, MN 55403

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hand Sanitizer with Aloe

with silicone holder

up & up

2 FL OZ (59.1 mL)

Package LabelPackage Label

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11673-085-162022-01-28C16284748780-1d6a99b39-67ee-a426-e053-dadaa90af4c2Hand Sanitizer with Aloe

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11673-085-16Hand Sanitizer with Aloe59.1 mL in 1 BOTTLE, PLASTICLIQUID59.11
11673-085-16Hand Sanitizer with Aloe1 in 1 CASELIQUID11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-085HAND SANITIZER WITH ALOE (ALCOHOL) LIQUID [TARGET CORPORATION]1Legacy NDC, 2 package rows20201219_d64dd273-20f0-4620-a235-755138b2aa83.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11673-08511673-085-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER INTERPOLYMER TYPE A (55000 CPS)59TL3WG5COIACT
TERT-BUTYL ALCOHOLMD83SFE959IACT
AMINOMETHYLPROPANOLLU49E6626QIACT
ALOE VERA LEAFZY81Z83H0XIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
DENATONIUM BENZOATE4YK5Z54AT2IACT
FD&C YELLOW NO. 5I753WB2F1MIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
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
b6ba4255-b3ff-e1f6-e053-2995a90a6ffad64dd273-20f0-4620-a235-755138b2aa832020-12-18WarningsExact identifier
spl id: b6ba4255-b3ff-e1f6-e053-2995a90a6ffa
spl set id: d64dd273-20f0-4620-a235-755138b2aa83

Reported adverse events (FAERS/openFDA)#

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