CHLORAPREP ONE-STEP- chlorhexidine gluconate and isopropyl alcohol solution

ChloraPrep One-Step by

Drug Labeling and Warnings

ChloraPrep One-Step by is a Otc medication manufactured, distributed, or labeled by CareFusion 213 LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Chlorhexidine gluconate 2% w/v

Isopropyl alcohol 70% v/v

Purposes

Antiseptic

Antiseptic

Use

for the preparation of the patient's skin prior to surgery or injection. Helps to reduce bacteria that potentially can cause skin infection.

Warnings

For external use only. Flammable, keep away from fire or flame.

• do not use with electrocautery procedures

Allergy alert:

This product may cause a severe allergic reaction.

Symptoms may include:

• wheezing/difficulty breathing
• shock
• facial swelling
• hives
• rash

If an allergic reaction occurs, stop use and seek medical help right away.

Do not use

• on patients allergic to chlorhexidine gluconate or any other ingredient in this product
• for lumbar puncture or in contact with the meninges
• on open skin wounds or as a general skin cleanser

When using this product

keep out of eyes, ears, and mouth. May cause serious or permanent injury if permitted to enter and remain. If contact occurs, rinse with cold water right away and contact a doctor.

Stop use and ask a doctor if

irritation, sensitization, or allergic reaction occurs. These may be signs of a serious condition.

Keep out of reach of children.

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

Directions

• use with care in premature infants or infants under 2 months of age. These products may cause irritation or chemical burns.
• maximal treatment area using three swabsticks sequentially is approximately 5 in. x 5 in. (160 cm 2)
• tear pouch at side notch to reveal applicator handles. Do not touch foam applicator tip. Place foam flat side down on the treatment area.
• completely wet the treatment area with antiseptic
• dry surgical sites (e.g., abdomen or arm): using each swabstick sequentially, use gentle repeated back-and-forth strokes for a total of 30 seconds. Allow the area to air dry for approximately 30 seconds. Do not blot or wipe away.
• moist surgical sites (e.g., inguinal fold): using each swabstick sequentially, use gentle repeated back-and-forth strokes for a total of 2 minutes. Allow the area to air dry for approximately 1 minute. Do not blot or wipe away.
• discard the applicator after a single use along with any portion of the solution not required to cover the prep area. It is not necessary to use the entire amount available.

Other information

• store between 15-30 ºC (59-86 °F)
• avoid freezing and excessive heat above 40 ºC (104 °F)

Inactive ingredient

USP purified water

Questions?

• www.chloraprep.com
• call 1-800-523-0502 (M-F 8 a.m.-5 p.m. CST)

Package/Label Principal Display Panel

PRINCIPAL DISPLAY PANEL-CARTON

5.25ml

TRIPLE

SWABSTICK

APPLICATORS

Clear

Do Not Reuse

Not made with natural rubber latex

40 packages

0.18 fl. oz. (5.25 ml) each

NDC: 054365-400-08

Cat. No. 260103

ChloraPrep ®

2% w/v chlorhexidine gluconate (CHG)

and 70% v/v isopropyl alcohol (IPA)

Patient Preoperative Skin Preparation

Non-Sterile Solution

Applicator is non-sterile

Professional Use Only

Store between 15-30 ºC (59-86 ºF)

Avoid freezing and excessive heat

above 40 ºC (104 ºF)

INGREDIENTS AND APPEARANCE

CHLORAPREP ONE-STEP 
chlorhexidine gluconate and isopropyl alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54365-400
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L)	CHLORHEXIDINE GLUCONATE	20 mg  in 1 mL
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: 54365-400-08	40 in 1 CARTON	06/10/2009
1		3 in 1 POUCH
1		1.75 mL in 1 APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
NDA	NDA021555	05/10/2005

Labeler - CareFusion 213 LLC (826496312)

Registrant - CareFusion 213 LLC (831684456)

Establishment
Name	Address	ID/FEI	Business Operations
CareFusion 213 LLC		826496312	analysis(54365-400) , manufacture(54365-400) , label(54365-400) , pack(54365-400)