QuickTouch Alcohol Prep Pad

Manufacturer
SLV Pharmaceuticals LLC
Effective date
2024-09-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:20:00

Label at a glance#

ProductQuickTouch Alcohol Prep Pad
Active ingredientISOPROPYL ALCOHOL
Label structure6 sections

Indications and uses

Antiseptic cleanser Kills harmful bacteria and germs First aid to help prevent infection

Dosage and administration

Use as part of your daily cleansing routine May be covered with a sterile bandage Store at room temperature 15°-30°C (59°-86°F) Avoid excessive heat

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol, 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic, Sterile Solution

Uses

DOSAGE & ADMINISTRATION SECTION

Antiseptic cleanser

Kills harmful bacteria and germs

First aid to help prevent infection

Warnings

WARNINGS SECTION

For External Use Only

Avoid contact with the eyes

If contact occurs, flush eyes with water

Flammable, keep away from fire or flame.

WARNINGS AND PRECAUTIONS SECTION

Do Not Use

OTC - DO NOT USE SECTION

With electrocautery prodedures

In the eyes

Stop Use and ask a doctor if

OTC - STOP USE SECTION

Irritation and redness develops

If condition persists for more than 72 hours, consult a physician

Discontinue use and consult a healthcare practitioner if

OTC - STOP USE SECTION

Irritation develops

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

INDICATIONS & USAGE SECTION

Use as part of your daily cleansing routine

May be covered with a sterile bandage

Other Information

OTHER SAFETY INFORMATION

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

Avoid excessive heat

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water

Quick Touch Alcohol Prep Pad

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Alcohol PadAlcohol Pad

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73317-4416-1QuickTouch Alcohol Prep Pad1 in 1 PACKETSWAB11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73317-4416QUICKTOUCH ALCOHOL PREP PAD (ALCOHOL PREP PADS) SWAB [SLV PHARMACEUTICALS LLC]11 package rows20240924_22babe01-af92-9e7e-e063-6394a90a7b9f.zip

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
73317-441673317-4416-1

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
ISOPROPYL ALCOHOLND2M416302ACTIB

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
22baf71e-2760-12b1-e063-6394a90a6fd022babe01-af92-9e7e-e063-6394a90a7b9f2024-09-22WarningsExact identifier
spl id: 22baf71e-2760-12b1-e063-6394a90a6fd0
spl set id: 22babe01-af92-9e7e-e063-6394a90a7b9f

Reported adverse events (FAERS/openFDA)#

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