FDA.reportPublic FDA data

Target Hand Sanitizer Clear Gel with Aloe, NDC-82442-031

Manufacturer
TARGET CORPORATION INC. | Apollo Health and Beauty Care
Effective date
2026-05-03
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:56:10

Label at a glance#

ProductEthanol
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

For personal hand hygiene to help prevent the spread of bacteria, and can be used in place of hand washing if soap and water are not available.

Dosage and administration

For occassional and personal use. Rub thoroughly into hands for at least 30 seconds. Allow to dry. Children under 6 should only use the product under adult supervision.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For personal hand hygiene to help prevent the spread of bacteria, and can be used in place of hand washing if soap and water are not available.

Warnings

WARNINGS SECTION

For External use only.

  • Flammable.
  • Keep away from source of heat or fire.

When using this product

OTC - WHEN USING SECTION

  • Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
  • Do not inhale or ingest.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation or redness develops and lasts.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • For occassional and personal use.
  • Rub thoroughly into hands for at least 30 seconds. Allow to dry.
  • Children under 6 should only use the product under adult supervision.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Fragrance (Parfum), Glycerin, Isopropyl Alcohol, Isopropyl Myristate, Tocopheryl Acetate, Water (Aqua).

Questions?

OTC - QUESTIONS SECTION

1-800-910-6874.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display PanelPrincipal Display Panel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82442-031-02Ethanol59 mL in 1 BOTTLE, PLASTICGEL593

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
82442-03182442-031-02

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
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
ISOPROPYL ALCOHOLND2M416302IACT
GLYCERINPDC6A3C0OXIACT
.ALPHA.-TOCOPHEROL ACETATE, D-A7E6112E4NIACT
WATER059QF0KO0RIACT
ALOE BARBADENSIS LEAF JUICERUE8E6T4NBIACT
FRAGRANCE CLEAN ORC0600327329LCV5BTFIACT
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
EthanolALCOHOLTARGET CORPORATION INC.28ef35a8-e6ca-9669-e063-6394a90abf8f2026-05-03WarningsExact identifier
ndc (package): 82442-031-02
ndc (product): 82442-031
ndc11 (package): 82442003102
spl id: 50f05b46-2822-f937-e063-6294a90addfc
spl set id: 28ef35a8-e6ca-9669-e063-6394a90abf8f