ISOPROPYL ALCOHOL SEPP- isopropyl alcohol solution
CareFusion 213 LLC

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.

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Active ingredient

Isopropyl alcohol 70% v/v, USP

Purpose

Antiseptic

Uses

for the preparation of the patient's skin prior to injection

Warnings

For external use only

Flammable: Keep away from fire or flame

Do not use with electrocautery procedures

Do not use

on patients with known allergies to isopropyl alcohol

When using this product

keep out of eyes, ears, and mouth

Stop use and ask a doctor if

irritation, sensitization, allergic reaction occurs. You may report side effects to FDA at 1-800-FDA-1088.

Keep out of reach of children.

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

Directions

remove Sepp. Hold in downward position and pinch center of Sepp to crush ampule.
apply isopropyl alcohol to venipuncture site starting at center and moving outward in concentric circles to periphery.
allow to dry. Discard unused components.

Other information

stove below 30 °C (86 °F)

Inactive ingredients

USP purified water

Questions?

Call 1-800-523-0502 (M-F 8 a.m.-5 p.m. CST)
www.carefusion.com

Package/Label Principal Display Panel

IPA Sepp Carton Primary Display Panel

Latex Free

2100 Applicators

(Net 0.67 ml each)

SEPPS®

CareFusion

Leawood, KS 66211

1.800.523.0502

Made in USA

WARNINGS: FOR EXTERNAL USE ONLY.

Do not use in the eyes.
Discontinue use if irritation and redness develop. If condition persists for more than 72 hours consult a physician.
Flammable, keep away from fire or flame.
Do not use with electrocautery procedures.

FOR SINGLE USE ONLY

FOR HOSPITAL & PROFESSIONAL USE ONLY

CONTENTS STERILE IF PRIMARY CONTAINER IS INTACT

STORE BELOW 30 °C OR 86 °F

ISOPROPYL ALCOHOL SEPP
isopropyl alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54365-170
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (ISOPROPYL ALCOHOL)	ISOPROPYL ALCOHOL	.70 mL in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER

Packaging
#	Item Code	Package Description
1	NDC:54365-170-01	200 in 1 CARTON
1		1 in 1 POUCH
1		0.67 mL in 1 APPLICATOR

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/01/1988

Labeler - CareFusion 213 LLC (826496312)

Establishment
Name	Address	ID/FEI	Business Operations
CareFusion 213 LLC		826496312	LABEL, MANUFACTURE, PACK

Revised: 06/2011

Document Id: 9d338f45-01b8-45cc-9a1a-15af40b6faaa

Set id: 597a86c0-99f3-4df6-be4a-208106a7799a

Version: 6

Effective Time: 20110601

CareFusion 213 LLC