Up & Up 826.000/826AA rev 1

Manufacturer
Target Corporation | Nice-Pak Products, LLC
Effective date
2026-04-21
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
full-release
Hydrated at
2026-06-01 01:54:25

Label at a glance#

ProductAlcohol
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

to decrease bacteria on the skin that could cause disease recommended for repeated use

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping for children under 6, use only under adult supervision not recommended for infants

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

  Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • to decrease bacteria on the skin that could cause disease
  • recommended for repeated use

Warnings

WARNINGS SECTION

For exterjnal use only: hands

Flammable, keep away from fire or flame

When using this product

OTC - WHEN USING SECTION

  • keep out of eyes.  In case of contact with eyues, flush thoroughly with water.
  • aoid contact with broken skin
  • do not inhale of ingest

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation and redness develop
  • condition persists 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

  • wet hands thoroughly with product and allow to dry without wiping
  • for children under 6, use only under adult supervision
  • not recommended for infants

Other information

OTHER SAFETY INFORMATION

  • do not store above 105° F
  • may discolor some fabrics
  • harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, carbomer, fragrance, glycerin, isopropyl myristate, Aloe barbadensis leaf juice, tocopheryl acetate, blue 1, yellow 5

ADVERSE REACTION

ADVERSE REACTIONS SECTION

*Effective at eliminating 99.99% of many common harmful germs and bacteria in as little as 15 seconds.

Dist. by Target Corp., Mpls., MN 55403

Made in U.S.A. with U.S. and foreign components

TM & ©2023 Target Brands, Inc.

Guest Servies: 1-800-910-6874

Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

kills 99.99% of germs*

moisturizing

hand sanitizer

with aloe

up & up™

2 FL OZ (59.1 mL)

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
247835ethanol 62 % Topical SolutionPSN10
247835ethanol 0.62 ML/ML Topical SolutionSCD10
247835ethanol 62 % Topical SolutionSY10
247835ethyl alcohol 62 % Topical SolutionSY10

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11673-826-16Alcohol59 mL in 1 BOTTLE, PLASTICLIQUID5910
11673-826-34Alcohol237 mL in 1 BOTTLE, PLASTICLIQUID23710
11673-826-45Alcohol946 mL in 1 BOTTLE, PLASTICLIQUID94610

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
11673-82611673-826-34, 11673-826-45, 11673-826-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
92026-02-18monthly-update2026-06-03 17:56:36

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
AlcoholALCOHOLTarget Corporation5c6be1e4-ae02-430c-8ed7-2148660da19d2026-04-21Warnings, Adverse reactionsExact identifier
ndc (package): 11673-826-16
ndc (package): 11673-826-34
ndc (package): 11673-826-45
ndc (product): 11673-826
ndc11 (package): 11673082616
ndc11 (package): 11673082634
ndc11 (package): 11673082645
spl id: 4ffdb678-aabd-4d99-e063-6394a90ac0b8
spl set id: 5c6be1e4-ae02-430c-8ed7-2148660da19d

Reported adverse events (FAERS/openFDA)#

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