STERILLIUM MED- alcohol liquid

Sterillium Med by

Drug Labeling and Warnings

Sterillium Med by is a Otc medication manufactured, distributed, or labeled by BODE Chemie GmbH. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Ethyl Alcohol 85% w/w

PURPOSE

Purpose

Antiseptic

INDICATIONS & USAGE

Uses

For handwashing to decrease bacteria on the skin.

Recommended for repeated use.

WARNINGS

Warnings

For external use only.

Flammable, keep away from fire or flame.

Do not use in or near the eyes or on mucous membranes.

In case of contact, rinse thoroughly with water.

Stop use and ask a dotor if

irritation and redness develop

condition persists for more than 72 hours

Keep out of reach of children.

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

DOSAGE & ADMINISTRATION

Directions

Apply to clean, dry hands, covering entire surface, including nails

Rub until dry

Supervise children in the use of this product

INACTIVE INGREDIENT

Inactive Ingredients

Glycerin, Methylethylketone, Myristyl Alcohol, n-Propyl Alcohol, Water

PRINCIPAL DISPLAY PANEL

Bode

Sterillium Med

Healthcare Personnel

Hand Antiseptic

85% w/w ethyl alcohol with moisturizers

Kills >99.999% of germs

in 15 seconds without water.

Leaves hands feeling soft and healthy.

Dermatologically tested.

Read Drug Facts panel before use.

Liquid formula with

95% natural ingredients

Lot:

Use by:

Questions? Call 1-800-MEDLINE

500 ml 16.91 fl. oz.

INGREDIENTS AND APPEARANCE

STERILLIUM MED 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65616-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	85 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
METHYL ETHYL KETONE (UNII: 6PT9KLV9IO)
MYRISTYL ALCOHOL (UNII: V42034O9PU)
PROPYL ALCOHOL (UNII: 96F264O9SV)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65616-005-02	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/26/2012
2	NDC: 65616-005-06	1000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	03/26/2012
3	NDC: 65616-005-08	50 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/26/2012
4	NDC: 65616-005-03	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	03/08/2013

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/26/2012	01/01/2021

Labeler - BODE Chemie GmbH (316039007)

Establishment
Name	Address	ID/FEI	Business Operations
BODE Chemie GmbH		316039007	manufacture(65616-005)