Sterillium Rub description, usages, side effects, indications, overdosage, supplying and lots more!

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Sterillium Rub

Bode Chemie Hamburg

Drug Facts




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredient                        Purpose

Ethanol 80% w/w.......................Antiseptic

Uses

Uses

surgical hand antiseptic

significantly reduces the number of micro-organisms on the hands and forearms prior to surgery or patient care

Warnings

For external use only.

Flammable, keep away from fire or flame.

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

When using this product and contact with eyes occurs, flush immediately with water.

Stop use and ask a doctor if

irritation and redness develop

conditions 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.

Directions

apply to clean dry hands

for the first use of the day, use a nail pick

dispense approx. 2 mL into hand, dip fingers of opposite hand into palm, working product under nails and into cuticles

repeat procedure with other hand

with hands still moist spread around the hand and lower 1/3 of the forearm

reapply the product to the hands, paying particular attention to fingers, cuticles, and interdigital spaces

following application, rub hands until dry

hands should remain moist for entire application time, approx. 2 minutes

Inactive Ingredients

Ethylhexyl Ethylhexanoate, Fragrance, Isohexadecane, Lanolin Alcohol, Myristyl Alcohol, PCA, Sodium PCA, Water.

Sterillium Rub

Procedural Scrub

Surgical Hand Antiseptic

80% ethyl alcohol w/w with emollients

Indication: Significantly reduces the number of micro-organisms on the hands andforearms prior to surgery or patient care.

Fast-acting.

Dermatologically tested.

Gentle to skin.

Read Drug Facts panel before use.

Lot:

Use by:

Questions? Call 1-800-MEDLINE, 7 a.m.-7 p.m. CST

1000 mL 33.8 fl. oz.

Sterillium Rub

Sterillium Rub

Surgical Hand Antiseptic LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:65616-001
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ALCOHOL ALCOHOL 80 mL

Inactive Ingredients

Ingredient Name Strength
MYRISTYL ALCOHOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:65616-001-01 100 in 1 BOTTLE, PLASTIC
2 NDC:65616-001-06 1000 in 1 BOTTLE, PUMP
3 NDC:65616-001-08 50 in 1 BOTTLE, SPRAY

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part333 2003-05-01


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Be sure to consult your doctor before taking any medication!
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