SANI-HANDS FOR KIDS- alcohol cloth

Sani-Hands by

Drug Labeling and Warnings

Sani-Hands by is a Otc medication manufactured, distributed, or labeled by Professional Disposables International, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Uses

• For hand washing to decrease bacteria on the skin.
• Recommended for repeated use.
• Dries in seconds.

Warnings

• Flammable, keep away from fire or flame.
• For external use only.
• Do not use in or contact the eyes.
• Discontinue use if irritation and redness develop. If condition persist for more than 72 hours consult a physician.
• If swallowed, get medical help or contact a Poison Control Center right away.

• Keep this out of reach of children unless under adult supervision.

Directions

• Tear open packet
• Open and unfold wipe.
  
• Thoroughly wipe hands, fingers and wrists. Be sure to use the entire wipe.
• For dirty hands, use first wipe to clean hands, then discard wipe; sanitize with second wipe.
• Discard after single use.

Other information

Lot No. and Expiration Date can be found on packet.

Dosage

For dirty hand, use first wipe to clean hands, then discard wipe; sanitize with second wipe. Discard after single use.

Inactive ingredients

Water, Propylene Glycol, Glycerin, Carbomer, Aminometyl Propanol, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate

SPL UNCLASSIFIED SECTION

Professional Disposables International, Inc.
2 Nice-Pak Park
Orangeburg, NY 10962-1376
www.sani-kids.com   Questions? Feedback?
Call us 1-800-444-6725 ext. 632
Made in USA

Principal Display Panel - 3000 Packets per Case

Sani
Professional Brand

SANI-HANDS(R)
for Kids

• Instant Hand Sanitizing Wipes
  
• Kills 99.99% of Germs
• Cleans better than gels

Contents: 3000 Packets per Case
7.75 x 5.0 in (19.68 x 12.7 cm)

Packet Label

Case Label

Active ingredient

Alcohol 65.9% by volume

Purpose

Antiseptic

INGREDIENTS AND APPEARANCE

SANI-HANDS  FOR KIDS
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10819-6003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M)	Alcohol	0.659 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10819-6003-4	3000 in 1 BOX

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/01/2007

Labeler - Professional Disposables International, Inc. (800777117)

Establishment
Name	Address	ID/FEI	Business Operations
Professional Disposables International, Inc.		800777117	manufacture