QUICKTOUCH ALCOHOL PREP PAD- alcohol prep pads swab

QuickTouch Alcohol Prep Pad by

Drug Labeling and Warnings

QuickTouch Alcohol Prep Pad by is a Otc medication manufactured, distributed, or labeled by SLV Pharmaceuticals LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Isopropyl Alcohol, 70% v/v

Purpose

Antiseptic, Sterile Solution

Uses

Antiseptic cleanser

Kills harmful bacteria and germs

First aid to help prevent infection

Warnings

For External Use Only

Avoid contact with the eyes

If contact occurs, flush eyes with water

Flammable, keep away from fire or flame.

Do Not Use

With electrocautery prodedures

In the eyes

Stop Use and ask a doctor if

Irritation and redness develops

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

Discontinue use and consult a healthcare practitioner if

Irritation develops

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away

Directions

Use as part of your daily cleansing routine

May be covered with a sterile bandage

Other Information

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

Avoid excessive heat

Inactive Ingredients

Water

Quick Touch Alcohol Prep Pad

INGREDIENTS AND APPEARANCE

QUICKTOUCH ALCOHOL PREP PAD 
alcohol prep pads swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73317-4417
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	0.7 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73317-4417-1	1 in 1 PACKET; Type 0: Not a Combination Product	09/16/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	09/16/2024

Labeler - SLV Pharmaceuticals LLC (081225162)

Registrant - SLV Pharmaceuticals LLC (081225162)