FDA.reportPublic FDA data

Up and up Alcohol prep pad

Manufacturer
Target Corporation | Nice-Pak Products, Inc. | Professional Disposables International, Inc.
Effective date
2020-06-25
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:24:15

Label at a glance#

ProductUp and up Alcohol prep pad
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Open packet Remove pad Appy topically as needed to cleanse intended area. Discard after single use.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropylic Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For preparation of the skin prior to an injection

Warnings

WARNINGS SECTION

For external use only.

Flammable, keep away from fire or flame.

Do not

OTC - DO NOT USE SECTION

  • use with electrocautery procedures
  • use in the eyes
  • apply to irritated skin

Stop use if

OTC - STOP USE SECTION

pain, irritation, redness, or swelling occurs, discontinue use and cnsult a physician.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Cener right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Open packet
  • Remove pad
  • Appy topically as needed to cleanse intended area. Discard after single use.

Other information

OTHER SAFETY INFORMATION

  • Contents sterile in unopened, undammaged pacakge
  • Store at room temperature 15-30ºC (59-86ºF)

Inactive ingredient

INACTIVE INGREDIENT SECTION

Purified water

Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Up and Up Alcohol Prep pad

antiseptic

sterile solution

applicator is sterile if he package is intact

hygienically cleanses

conveninet and disposable

packet label: labellabel

box containing 200 packets: box 200ctbox 200ct

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11673-40611673-406-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
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
eca82586-707c-249e-e053-2a95a90a9c2329284788-5675-6f0d-e054-00144ff8d46c2022-11-04WarningsExact identifier
spl set id: 29284788-5675-6f0d-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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