NDC 82442-002, Target Hand Sanitizer Clear Gel

Manufacturer
TARGET CORPORATION INC. | Apollo Health and Beauty Care
Effective date
2026-09-24
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
daily-update
Hydrated at
2026-09-29 01:03:25

Label at a glance#

ProductAlcohol
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

For personal hand hygine 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. Allo to dry. Children under 6 years should be supervised when using this product.

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 hygine 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.

Do not use

OTC - DO NOT USE SECTION

  • On infants less than 2 months of age.
  • On open skin wounds
  • On broken or damaged skin.

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor

OTC - WHEN USING SECTION

if 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 Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • For occassional and Personal use.
  • Rub thoroughly into hands for at least 30 seconds. Allo to dry.
  • Children under 6 years should be supervised when using this product.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, AMP-Acrylates/vinyl Isodecanoate Crosspolymer, Fragrance (Parfum), Glycerin, Isopropyl Alcohol, Isopropyl Myristate, PEG-6, Tocopheryl Acetate, Water (Aqua).

Questions

OTC - QUESTIONS SECTION

1-800-910-6874

Package 2 FL Oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

2 oz2 oz

Package 8 FL Oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package 8 FL OZ

06-2722206-27222

Package 32 FL Oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

32 OZ32 OZ

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130085239182291GTIN-13: 0085239182291
EAN-13: 0085239182291
GTIN-12: 085239182291
UPC-A: 085239182291
GTIN storage (14 digits): 00085239182291
06-25978.jpg
BarcodeEAN-130085239182307GTIN-13: 0085239182307
EAN-13: 0085239182307
GTIN-12: 085239182307
UPC-A: 085239182307
GTIN storage (14 digits): 00085239182307
06-27222.jpg
BarcodeEAN-130085239182314GTIN-13: 0085239182314
EAN-13: 0085239182314
GTIN-12: 085239182314
UPC-A: 085239182314
GTIN storage (14 digits): 00085239182314
06-25984.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82442-00282442-002-02, 82442-002-08, 82442-002-32

Ingredients#

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

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

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32026-05-03full-release2026-06-01 01:56:08

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
50f0362d-b5fc-48c0-e063-6394a90af29b092ed157-3a25-edce-e063-6394a90a93472026-05-03WarningsExact identifier
spl set id: 092ed157-3a25-edce-e063-6394a90a9347

Reported adverse events (FAERS/openFDA)#

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