AMERICAN INFECTION CONTROL ANTISEPTIC HAND WIPES- alcohol cloth

American Infection Control Antiseptic Hand Wipes by

Drug Labeling and Warnings

American Infection Control Antiseptic Hand Wipes by is a Otc medication manufactured, distributed, or labeled by American Infection Control, Inc., Sapro Temizlik Urunleri Sanayi ve Ticaret A.S.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

DRUG FACTS

Active Ingredient

Ethyl Alcohol 62% (v/v)

Purpose

Antiseptic

Uses:

For handwashing to decrease bacteria on the skin after assisting ill persons, before contact with a person under medical care or treatment, or after changing diapers, and to remove light soil and germs from the skin. Not for use on intimate parts of the body, as the alcohol may sting or cause inflammation.

WARNINGS

For external use only.

• Do not use in eyes. In case of eye contact, immediately flush with water and seek medical advice.
• Not for use on broken or irritated skin, unless recommended by a health care professional for wound or first aid cleansing.
• Discontinue use and seek medical attention if skin irritation or redness develops.

Keep out of reach of children.

If swallowed, get medical help or contact a poison control center immediately.

Directions:

Snap open lid. Remove wipes for use. Wipe hands and wrists thoroughly, using more than one wipe if necessary. Snap lid closed between uses to preserve moisture and freshness of the product. When pack is empty dispose of the empty packaging materials properly or recycle with other plastic items. FLAMMABLE. KEEP AWAY FROM HIGH HEAT OR DIRECT FLAME

Inactive Ingredients:

Aloe Barbadensis Extract, Propylene Glycol, Purified Water.

PRINCIPAL DISPLAY PANEL

Principal Display Panel – Package Label

ANTISEPTIC HAND WIPES

Kills Over WON'T
99.99% DRY
of Harmful HANDS
Germs & WITH
Bacteria REPEATED
FRAGRANCE FREE USE

80 PRE-MOISTENED WIPES (6 in. x 7 in.)

INGREDIENTS AND APPEARANCE

AMERICAN INFECTION CONTROL ANTISEPTIC HAND WIPES 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76113-012
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M)	Alcohol	.62 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Aloe Vera Leaf (UNII: ZY81Z83H0X)
Propylene Glycol (UNII: 6DC9Q167V3)
Water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76113-012-54	20 in 1 CASE
1		228 mL in 1 PACKAGE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	02/15/2012

Labeler - American Infection Control, Inc. (967579934)

Establishment
Name	Address	ID/FEI	Business Operations
Sapro Temizlik Urunleri Sanayi ve Ticaret A.S.		365536965	MANUFACTURE(76113-012) , ANALYSIS(76113-012)