FDA.reportPublic FDA data

82442-088-07, Target up and up Antibacterial Liquid Hand Soap

Manufacturer
TARGET CORPORATION INC. | Apollo Health and Beauty Care
Effective date
2026-05-08
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:56:39

Label at a glance#

ProductUP and UP
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

For hand washing to decrease bacteria on the skin.

Dosage and administration

Apply onto dry hands. Lather and rinse thoroughly with water.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride (0.13%)

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

  • For hand washing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

  • Avoid contact with eyes. In case of contact, flush with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or redness develops and lasts for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

if swallowed, get medical help or contact a Poison Control center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply onto dry hands.
  • Lather and rinse thoroughly with water.

Inactive Ingredients.

INACTIVE INGREDIENT SECTION

Water (Aqua), Cocamidopropyl Betaine, Hydroxyethylcellulose, Tetrasodium EDTA, Glycerin, Citric Acid, Methylchloroisothiazolinone, Methylisothiazolinone, Poloxamer 124, Fragrance (Parfum), Red 40 (CI 16035), Yellow 5 (CI 19140), Red 33 (CI 17200).

Questions

OTC - QUESTIONS SECTION

1-800-910-6874

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display PanelPrincipal Display Panel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN5
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD5
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY5
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY5

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130191907923223GTIN-13: 0191907923223
EAN-13: 0191907923223
GTIN-12: 191907923223
UPC-A: 191907923223
GTIN storage (14 digits): 00191907923223		PDP.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82442-088-07UP and UP222 mL in 1 BOTTLE, PLASTICLIQUID2225

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82442-08882442-088-07

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
HYDROXYETHYLCELLULOSET4V6TWG28DIACT
FRAGRANCE CLEAN ORC0600327329LCV5BTFIACT
FD&C RED NO. 40WZB9127XOAIACT
D&C RED NO. 339DBA0SBB0LIACT
POLOXAMER 1241S66E28KXAIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
TETRASODIUM EDTAMP1J8420LUIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
GLYCERINPDC6A3C0OXIACT
CITRIC ACID2968PHW8QPIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22025-10-31monthly-update2026-06-03 17:38:20

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
UP and UPBENZALKONIUM CHLORIDETARGET CORPORATION INC.39855595-cd79-a116-e063-6294a90a96382026-05-08WarningsExact identifier
ndc (package): 82442-088-07
ndc (product): 82442-088
ndc11 (package): 82442008807
spl id: 51531f24-f43f-f7d9-e063-6294a90a0394
spl set id: 39855595-cd79-a116-e063-6294a90a9638

Reported adverse events (FAERS/openFDA)#

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