Alcohol Prep Pad: Package Insert and Label Information

ALCOHOL PREP PAD- isopropyl alcohol swab
NDC National Distribution & Contracting, Inc.

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.

Drug Facts

Active Ingredients

Isopropyl Alcohol 70%

Purpose

Antiseptic Cleanser

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 procedures
• In the Eyes. If contact occurs, flush eyes with water
  

Stop Use

If irritation and redness develop. If condition persists, consult your health care practitioner.

Keep out of reach of children

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

Directions

Wipe injection site vigorously and discard.

Other Information

Store at Room Temperature 15 — 30 C (59 — 86 F)

Inactive Ingredient

purified water

PRINCIPAL DISPLAY PANEL — 100 Pouch Box Label

REF: P902050

Sterile

Alcohol Prep Pads

Large (1.75 IN × 3.5 IN)

For Professional and Hospital Use

Sterile unless package is opened or damaged.
Do not resterilize.

Pro Advantage ^®
by NDC

10 boxes/case | 100/box

ALCOHOL PREP PAD isopropyl alcohol swab

Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43128-050 Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (ISOPROPYL ALCOHOL) ISOPROPYL ALCOHOL 0.7 mL in 1 mL

Inactive Ingredients Ingredient Name Strength WATER

Packaging # Item Code Package Description Multilevel Packaging 1 NDC:43128-050-01 100 POUCH in 1 BOX contains a POUCH 1 1 mL in 1 POUCH This package is contained within the BOX (43128-050-01) 2 NDC:43128-050-02 200 POUCH in 1 BOX contains a POUCH 2 1 mL in 1 POUCH This package is contained within the BOX (43128-050-02)

Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 12/15/2011

Labeler — NDC National Distribution & Contracting, Inc. (009831413)

Establishment
Name	Address	ID/FEI	Operations
Dukal		421317073	manufacture (43128-050)

Revised: 03/2023 NDC National Distribution & Contracting, Inc.