FDA.reportPublic FDA data

Alcohol Prep Pad

Manufacturer
Target Corporation
Effective date
2010-02-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:23:30

Label at a glance#

ProductAlcohol Prep Pad
Active ingredientIsopropyl alcohol
Label structure9 sections

Dosage and administration

Wipe injection site vigorously and discard.

Storage and handling

Store at room temperature 15°- 30° C (59° - 86° F)

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Isopropyl 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 use

OTC - DO NOT USE SECTION

  • with electrocautery procedures
  • in the eyes

Stop use

OTC - STOP USE SECTION

if irritation and redness develop. If condition persists for more than 72 hours, consult a doctor.

OTC - ASK DOCTOR/PHARMACIST SECTION

OTC - WHEN USING SECTION

OTC - ASK DOCTOR SECTION


WARNINGS SECTION

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

Wipe injection site vigorously and discard.

OTHER INFORMATION

STORAGE AND HANDLING SECTION

Store at room temperature 15°- 30° C (59° - 86° F)

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

purified water

Questions?

OTC - QUESTIONS SECTION

Call 1-800-910-6874

PACKAGE INFORMATION

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

up and up

NDC 11673-600-10

alcohol prep pads
70% isopropyl alcohol

Compare to BD®*

antiseptic for preparation of skin prior to injection

100 count

100 INDIVIDUALLY WRAPPED PADS

Distributed by Target Corporation
Minneapolis, MN 55403
Made in U.S.A.

© 2009 Target Brands, Inc.
All Rights Reserved
Shop Target.com

*This product is not manufactured or distributed by Becton Dickinson and Company, owner of the registered trademark BD®.

image of cartonimage of carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
797544isopropyl alcohol 70 % Medicated PadPSN1
797544isopropyl alcohol 0.7 ML/ML Medicated PadSCD1
797544isopropyl alcohol 70 % Medicated PadSY1
797544isopropyl alcohol 70 % Topical ClothSY1
797544isopropyl alcohol 70 % Topical SwabSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11673-600-102019-10-21C16284748780-1956f9ecf-d587-621f-e053-dbdaa90a74adDRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11673-600-10Alcohol Prep Pad1 in 1 PACKETSWAB11
11673-600-10Alcohol Prep Pad100 in 1 BOXSWAB1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-600ALCOHOL PREP PAD (ISOPROPYL ALCOHOL) SWAB [TARGET CORPORATION]1Legacy NDC, 2 package rows20100202_e9bf3004-f9c8-4881-ae4a-8e902840f4ce.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
11673-600-10EA - Each11673-6001722a50f-68d0-48bd-9747-8c16e1f9cb6712012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Isopropyl alcoholACTIVE INGREDIENTND2M4163021
Isopropyl alcoholACTIVE MOIETYND2M4163021
waterINACTIVE INGREDIENT059QF0KO0R1

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11673-60011673-600-10

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
Isopropyl alcoholND2M416302ACTIB
water059QF0KO0RIACT

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
112e2e0e-b96b-4753-8df1-800b0e3ca23fe9bf3004-f9c8-4881-ae4a-8e902840f4ce2010-02-01WarningsExact identifier
spl id: 112e2e0e-b96b-4753-8df1-800b0e3ca23f
spl set id: e9bf3004-f9c8-4881-ae4a-8e902840f4ce

Reported adverse events (FAERS/openFDA)#

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