76162-808 TopCare IPA Prep Pads

Manufacturer: Topco Associates | Medline Industries, LP
Effective date: 2026-09-02
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: daily-update
Hydrated at: 2026-09-05 01:01:00

Label at a glance#

ProductAlcohol Prep Pads

Active ingredientISOPROPYL ALCOHOL

Label structure9 sections

Indications and uses

For preparation of the skin prior to injection First aid antiseptic to help prevent infection in minor cuts, scrapes and burns.

Dosage and administration

Apply to skin as needed. Discard after single use.

Storage and handling

Protect from freezing and avoid excessive heat. Not made with Natural Rubber Latex.

Contacts and useful links#

PhoneLabel contact1-888-423-0139

Websitewww.topcarebrand.com

www.topcarebrand.com

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol, 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For preparation of the skin prior to injection
First aid antiseptic to help prevent infection in minor cuts, scrapes and burns.

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.
Longer than one week unless directed by a physician.

When using this product

OTC - WHEN USING SECTION

Do not get in eyes.
Do not apply over large areas of the body.
In case of deep or puncture wounds, animal bites or serious burns, consult a doctor.

Stop use and ask a doctor if

OTC - STOP USE SECTION

Irritation and redness develop.
Condition gets worse or persists for more than 72 hours.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If accidentally swallowed, seek medical assistance or immediately contact a Poison Control Center.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to skin as needed.
Discard after single use.

Other information

STORAGE AND HANDLING SECTION

Protect from freezing and avoid excessive heat.
Not made with Natural Rubber Latex.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water

Manufacturer information

SPL UNCLASSIFIED SECTION

DISTRIBUTED BY TOPCO ASSOCIATES LLC

ITASCA, IL 60143

©TOPCO MDLA1024

QUESTIONS? 1-888-423-0139

topcare@topco.com www.topcarebrand.com

PACKAGED IN CHINA WITH COMPONENTS FROM TAIWAN

REF TOP090734V2 V1 RK24SXM

Package label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Box labelEach label

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
QR code link	QR Code	topbrnds.com/490zyw		TOP090734V2 box.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1	Product name	1	20230829

Products#

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

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

Alcohol Prep Pads
Isopropyl Alcohol
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
76162-808	76162-808-30

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
ISOPROPYL ALCOHOL	ND2M416302	ACTIB
WATER	059QF0KO0R	IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
2	2025-05-22	full-release	2026-06-01 01:01:27

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
Alcohol Prep Pads	ISOPROPYL ALCOHOL	Topco Associates	2642298f-607e-fdca-e063-6394a90a69d9	2026-09-02	Warnings	Exact identifier ndc (package): 76162-808-30 ndc (product): 76162-808 ndc11 (package): 76162080830 spl id: 5a85d4f5-0086-9103-e063-6394a90a6f31 spl set id: 2642298f-607e-fdca-e063-6394a90a69d9

Reported adverse events (FAERS/openFDA)#

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