Up and Up 70 Isopropyl Alcohol Wipes

Manufacturer: Target Corporation
Effective date: 2023-10-17
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 23:56:52

Label at a glance#

ProductUp and Up 70 Isopropyl Alcohol Wipes

Active ingredientISOPROPYL ALCOHOL

Label structure8 sections

Dosage and administration

• clean the affected area • apply product on the affected area of the body 1 to 3 times a day • may be covered with a sterile bandage • if bandaged, let dry first

Contacts and useful links#

PhoneLabel contact1-800-910-6874

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

First aid antiseptic

Use

INDICATIONS & USAGE SECTION

first aid to help prevent the risk of infection in:

• minor cuts • scrapes • burns

Warnings

WARNINGS SECTION

For external use only.

Flammable keep away from fire or flame, heat, spark, electrical

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

• deep or puncture wounds • animal bites • serious burns

When using this product

OTC - WHEN USING SECTION

• do not get in eyes • do not apply over large areas • do not use longer than 1 week unless directed by a doctor

Stop use and ask a doctor if

OTC - STOP USE SECTION

condition persists or gets worse.

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

• clean the affected area • apply product on the affected area of the body 1 to 3 times a day • may be covered with a sterile bandage • if bandaged, let dry first

Other information

SPL UNCLASSIFIED SECTION

• do not apply internally. • keep canister tightly closed and stored at room temperature • hold away from face when opening.

Inactive ingredient

INACTIVE INGREDIENT SECTION

purified water

Questions or comments?

OTC - QUESTIONS SECTION

Call 1-800-910-6874

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Updated label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
797544	isopropyl alcohol 70 % Medicated Pad	PSN	3
797544	isopropyl alcohol 0.7 ML/ML Medicated Pad	SCD	3
797544	isopropyl alcohol 70 % Medicated Pad	SY	3
797544	isopropyl alcohol 70 % Topical Cloth	SY	3
797544	isopropyl alcohol 70 % Topical Swab	SY	3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
11673-326-40	Up and Up 70 Isopropyl Alcohol Wipes	40 in 1 CANISTER	CLOTH	40		3
11673-326-40	Up and Up 70 Isopropyl Alcohol Wipes	4.7 mL in 1 PATCH	CLOTH	4.7		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
11673-326	UP AND UP 70 ISOPROPYL ALCOHOL WIPES (ISOPROPYL ALCOHOL) CLOTH [TARGET CORPORATION]	3	Current NDC, Legacy NDC, 2 package rows	20231018_becc8fe3-eaf5-4429-b462-a87dd09c4db8.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

Up and Up 70 Isopropyl Alcohol Wipes
ISOPROPYL ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
11673-326	11673-326-40

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
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ISOPROPYL ALCOHOL	ND2M416302	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Up and Up 70 Isopropyl Alcohol Wipes	ISOPROPYL ALCOHOL	Target Corporation	becc8fe3-eaf5-4429-b462-a87dd09c4db8	2023-10-17	Warnings	Exact identifier ndc (package): 11673-326-40 ndc (product): 11673-326 ndc11 (package): 11673032640 spl id: 07e5643b-23f5-ed55-e063-6294a90a4761 spl set id: becc8fe3-eaf5-4429-b462-a87dd09c4db8

Reported adverse events (FAERS/openFDA)#

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