ALCOSCRUB HAND CLEANER- alcohol liquid

Alcoscrub by

Drug Labeling and Warnings

Alcoscrub by is a Otc medication manufactured, distributed, or labeled by Erie Scientific, LLC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ethyl Alcohol 62 % v/v

PURPOSE

For handwashing  to decrease bacteria on skin.

Keep Out of Reach of Children

If swallowed, contact a physician or poison center

Indications & Usage Section

For hand cleaning to decrease bacteria on skin

WARNINGS

Flammable. Keep away from heat of flames. For external use only. Do not use in the eyes.

Discontinue use if redness and irritation develop.  If condition persists for more than 72 hours, consult a physician.  If swallowed, contact a physician or poison control center.  Keep out of the reach of children.

Dosage & Administration Section

Apply a small amount to palm.  Briskly rub, covering hands with product until dry.

Inactive ingredients

Water, Glycerin, Carbomer, Propylene glycol, Isopropyl Myristate, Triethanolamine, Aloe Barbadensis Leaf, Tocopheryl acetate

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ALCOSCRUB  HAND CLEANER
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55863-700
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	1 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Glycerin (UNII: PDC6A3C0OX)
Propylene Glycol (UNII: 6DC9Q167V3)
Isopropyl Myristate (UNII: 0RE8K4LNJS)
Aloe Vera Flower (UNII: 575DY8C1ER)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
Trolamine (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55863-700-04	118 mL in 1 BOTTLE
2	NDC: 55863-700-16	472 mL in 1 BOTTLE
3	NDC: 55863-700-27	800 mL in 1 POUCH
4	NDC: 55863-700-32	944 mL in 1 BOTTLE, PUMP

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/03/2009

Labeler - Erie Scientific, LLC. (361605223)