PDI SANI-HANDS INSTANT HAND SANITIZING WIPES- alcohol cloth

PDI Sani-Hands Instant Hand Sanitizing Wipes by

Drug Labeling and Warnings

PDI Sani-Hands Instant Hand Sanitizing Wipes by is a Otc medication manufactured, distributed, or labeled by Professional Disposables International, Inc., Professonal Disposables International, Inc, Guy & O'Neill, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Uses

• Antiseptic
  
• 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 immediately.

Keep out of reach of children

unless under adult supervision.

Directions

• Peel back label slowly
• Pull out wipe and reseal label
• Unfold and use
• Wipe hands, fingers, interdigital areas and wrists thoroughly with towelettes. Be sure to utilize the entire wipe surface. Allow to dry.
• If hands are visibly soiled or contaminated, use first wipe to clean hands, then discard wipe. Sanitize with a second wipe.
  
• Discard after single use.

Other information

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

Dosage

Use first wipe to clean hands, then discard wipe. Sanitize with a second wipe.

Inactive ingredients

Water, Propylene Glycol, Glycerin, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate

Manufactured for:

Professional Disposables International, Inc.
Orangeburg, NY 10962-1376 - USA - 1-800-999-6423
Made in USA

www.pdipdi.com

Active ingredient

Alcohol 65.9% by volume

Purpose

Antiseptic

Principal Display Panel - 20 Count

lid:

flowrap:

INGREDIENTS AND APPEARANCE

PDI SANI-HANDS INSTANT HAND SANITIZING WIPES 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10819-5808
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.659 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10819-5808-1	83 mL in 1 PACKAGE; Type 0: Not a Combination Product	12/01/2011

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/25/2011

Labeler - Professional Disposables International, Inc. (800777117)

Registrant - Professonal Disposables International, Inc (800777117)

Establishment
Name	Address	ID/FEI	Business Operations
Guy & O'Neill, Inc.		926830563	manufacture(10819-5808)