PDI ALCOHOL PREP PAD STERILE LARGE AND MEDIUM- alcohol cloth

PDI Alcohol Prep Pad Sterile by

Drug Labeling and Warnings

PDI Alcohol Prep Pad Sterile by is a Otc medication manufactured, distributed, or labeled by Professional Disposables International Inc, Professional Disposables International inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Isopropyl Alcohol 70% v/v

Purpose

Antiseptic

Use

For preparation of skin prior to an injection

Warnings

For external use only.

Flammable, keep away from fire or flame.

Do not

• use with electrocautery preocedures
• use in the eyes
• apply on irritated skin

Stop use if

pain, irritation, redness or swelling occurs. discontinue use and consult a physician.

Keep out of reach of children

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

Directions

Wet topically and discard after single use

Other information

Store at room temperature (15-30ºC) (59-86ºF)

Inactive ingredient

Purified Water

Principal display panel

Alcohol Prep Pad

Sterile

Medium or Large

Antiseptic

Sterile solution

Applicator is sterile if package is intact

For Hospital and Home Use Settings

Dispose of used wipes in trash receptacle. Do not flush.

Professional Disposables International, Inc.
Orangeburg, NY 10962-1376
USA - 1800-999-6423
www.pdipdi.com

Packet Medium:

Box Medium:

Packet Large:

Box Large:

INGREDIENTS AND APPEARANCE

PDI ALCOHOL PREP PAD STERILE  LARGE AND MEDIUM
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10819-3914
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	0.3 mL  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10819-3914-2	100 in 1 BOX	01/01/1972
1		1.6 mL in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 10819-3914-1	200 in 1 BOX	01/01/1972
2		0.62 mL in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/01/1972

Labeler - Professional Disposables International Inc (800777117)

Registrant - Professional Disposables International inc (800777117)

Establishment
Name	Address	ID/FEI	Business Operations
Professional Disposables International Inc		800777117	manufacture(10819-3914)