DUKAL STERILE ALCOHOL PREP PAD- isopropyl alcohol swab

Dukal Sterile Alcohol Prep Pad by

Drug Labeling and Warnings

Dukal Sterile Alcohol Prep Pad by is a Otc medication manufactured, distributed, or labeled by Dukal Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active Ingredients

Isopropyl Alcohol 70%

Purpose

Antiseptic Cleanser

PURPOSE

Use

For Preparation of Skin prior to an injection

INDICATIONS & USAGE

Apply topically as needed to cleanse

WARNINGS

Warnings

• For External Use Only
• Flammable, Keep away from fire or flame
  

DO NOT USE

Do Not Use

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

STOP USE

Stop Use

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

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

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

DOSAGE & ADMINISTRATION

Other Information

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

STORAGE AND HANDLING

Other Information

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

INACTIVE INGREDIENT

Inactive Ingredient

purified water

PRINCIPAL DISPLAY PANEL

Reorder 853

Dukal Corporation

NDC: 65517-0002-1

Sterile

ALCOHOL PREP PAD

Saturated with 70% Isopropyl Alcohol

For External Use Only

Sterility guaranteed unless package is damaged or open.

1 / Pouch Latex 2

Dukal Corporation 631-656-3800

Ronkonkoma, NY 11779

www.dukal.com

Made in China

PRINCIPAL DISPLAY PANEL

Reorder 853

Dukal Corporation

NDC: 65517-0002-1

Sterile

ALCOHOL PREP PAD

Saturated with 70% Isopropyl Alcohol

For External Use Only

Sterility guaranteed unless package is damaged or opened.

Latex 2

1 / Pouch

Dukal Corporation 631-656-3800

Ronkonkoma, NY 11779

www.dukal.com

Made in USA

INGREDIENTS AND APPEARANCE

DUKAL STERILE ALCOHOL PREP PAD 
isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65517-0002
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  in 1 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65517-0002-1	0.4 mL in 1 POUCH; Type 0: Not a Combination Product	01/01/2000

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/01/2000

Labeler - Dukal Corporation (791014871)