ISOPROPYL ALCOHOL SEPP- isopropyl alcohol solution

Isopropyl Alcohol Sepp by

Drug Labeling and Warnings

Isopropyl Alcohol Sepp by is a Otc medication manufactured, distributed, or labeled by CareFusion 213 LLC, CareFusion 2200, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Isopropyl alcohol 70% v/v, USP

Purpose

Antiseptic

Use

•   for the preparation of the 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

• In the eyes
• 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, or 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

• 1 remove the applicator wrapper. Do not touch the applicator tip.
• 2 with the applicator tip facing downward, pinch the barrel of the applicator ONCE to release the antiseptic.
• 3 press the applicator tip against the patient’s skin. With gentle back and forth actions apply solution to the treatment area.
• 4 the area covered should be allowed to dry naturally.
• 5 discard after single use

Other information

•   store below 30 °C (86 °F)

Inactive ingredients

•   USP purified water

Questions?

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

Package/Label Principal Display Panel

IPA Sepp Carton Primary Display Panel

INGREDIENTS AND APPEARANCE

ISOPROPYL ALCOHOL SEPP 
isopropyl alcohol solution

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

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	.70 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: 54365-170-01	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)

Registrant - CareFusion 2200, Inc (832696038)

Establishment
Name	Address	ID/FEI	Business Operations
CareFusion 213 LLC		826496312	LABEL(54365-170) , MANUFACTURE(54365-170) , PACK(54365-170)