ALCOHOL PREP PAD- isopropyl alcohol swab

Alcohol Prep pad by

Drug Labeling and Warnings

Alcohol Prep pad by is a Otc medication manufactured, distributed, or labeled by NDC National Distribution & Contracting, Inc., Dukal. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

Isopropyl Alcohol 70%

Purpose

Antiseptic Cleanser

Use

For Preparation of Skin prior to an injection

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.

Directions

Wipe injection site vigorously and discard.

STORAGE AND HANDLING

Other Information

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

INACTIVE INGREDIENT

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

INGREDIENTS AND APPEARANCE

ALCOHOL PREP PAD 
isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 43128-050
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: 43128-050-01	100 in 1 BOX	12/15/2011
1		1 mL in 1 POUCH; Type 0: Not a Combination Product
2	NDC: 43128-050-02	200 in 1 BOX	12/15/2011
2		1 mL in 1 POUCH; 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	12/15/2011

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

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