Alcohol Prep Pads

Manufacturer: QUEST USA CORP
Effective date: 2024-12-10
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 00:41:49

Label at a glance#

ProductAlcohol Prep Pads

Active ingredientISOPROPYL ALCOHOL

Label structure9 sections

Indications and uses

First aid to help reduce the risk of infection in minor cuts, scrapes, and burns.

Dosage and administration

Apply to skin as needed. Discard after single use. Children under 6 years of age should be supervised by an adult when using this product.

Storage and handling

Store in a cool, dry place, between 15°-30°C(59°F-86°F). Avoid freezing and excessive heat above 40°C(104°F).

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

Antiseptic

Uses

INDICATIONS & USAGE SECTION

First aid to help reduce the risk of infection in minor cuts, scrapes, and burns.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame.

Stop use and ask a doctor

OTC - ASK DOCTOR SECTION

if the condition persists or gets worse. Do not use longer than 1 week unless directed by a doctor.

Do not use

OTC - DO NOT USE SECTION

in the eyes or apply over large areas of the body. In case of deep or puncture wounds, animal bites, or serious bums, consult a doctor.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.If accidentally swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to skin as needed.
Discard after single use.
Children under 6 years of age should be supervised by an adult when using this product.

Other information

STORAGE AND HANDLING SECTION

Store in a cool, dry place, between 15°-30°C(59°F-86°F).
Avoid freezing and excessive heat above 40°C(104°F).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water

Questions?

OTC - QUESTIONS SECTION

Call 1-800-910-6874

Alcohol Prep Pads

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Alcohol Prep Pad Label

DailyMed Product Concepts#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
78691-026-01	2025-07-29	C162847	48780-1	3b156c62-2eda-fb37-e063-e6dba90a4e07	up&up Alcohol Prep Pads

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
78691-026-01	Alcohol Prep Pads	200 in 1 BOX	SWAB	200		2
78691-026-01	Alcohol Prep Pads	1 g in 1 POUCH	SWAB	1		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
78691-026	ALCOHOL PREP PADS (ISOPROPYL ALCOHOL, ALCOHOL PREP PADS) SWAB [QUEST USA CORP]	2	2 package rows	20241212_1ee676de-0044-6e20-e063-6294a90aaaf5.zip

Products#

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

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

Alcohol Prep Pads
Isopropyl Alcohol, Alcohol Prep Pads
WATER
ISOPROPYL ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78691-026	78691-026-01

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
28f3781c-4ad4-dd53-e063-6394a90a65c1			1ee676de-0044-6e20-e063-6294a90aaaf5	2024-12-10	Warnings	Exact identifier spl id: 28f3781c-4ad4-dd53-e063-6394a90a65c1 spl set id: 1ee676de-0044-6e20-e063-6294a90aaaf5

Reported adverse events (FAERS/openFDA)#

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