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PDI Alcohol Prep Pad Sterile Large and Medium

Dosage form: cloth
Ingredients: Alcohol 0.70mL in 1mL
Labeler: Professional Disposables International, Inc.
NDC Code: 10819-3914

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.


Active Ingredient

Isopropyl Alcohol 70% v/v




For preparation of the skin prior to an injection


For external use only.
Flammable, keep away from fire or flame.
Do not

  • use with electrocautery procedures
  • use in the eyes
  • apply to 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.


  • Open packet
  • Remove pad
  • Apply topically as needed to cleanse intended area. 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 solution

Applicator is sterile if package is intact

Large and Medium

For Professional and Hospital Use

Professional Disposables International, Inc.
Orangeburg, NY 10962-1376
USA - 1800-999-6423    Made in USA

100 Packets per Box (Large)
200 Packets per Box (Medium)

Large Packet Label

Large Box Label

Medium Packet Label

Medium Box Label

Dosage & Administration

See box for additional information.

alcohol cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10819-3914
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Alcohol (Alcohol) Alcohol0.70 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water0.30 mL  in 1 mL
#Item CodePackage Description
1NDC:10819-3914-2100 PACKET (PACKET) in 1 BOX
11.6 mL in 1 PACKET
2NDC:10819-3914-1200 PACKET (PACKET) in 1 BOX
20.62 mL in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/01/1972
Labeler - Professional Disposables International, Inc. (800777117)
Professional Disposables International, Inc.800777117manufacture(10819-3914)

Revised: 12/2014
Professional Disposables International, Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.