PDI SANI HANDS- instant hand sanitizing wipes cloth

PDI Sani Hands by

Drug Labeling and Warnings

PDI 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]

Active ingredient

Alcohol 70% by volume

Purpose

Antiseptic

Uses

• Antiseptic.
• For handwashing 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 conditions persist for more than 72 hours, consult a physician.

Keep this out of reach of children

unless under adult supervision.

if swallowed, get medical help or contact a Poison Control Center immediately

Directions

• Peel back label slowly.
• Pull out wipe and reseal label.
• Unfold and use.
• Wipe hands, fingers, interdigital areas and wrists thoroughly with towelette. 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.

inactive ingredients

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

Principal Display panel

Reseal lid:

Flowrap:

INGREDIENTS AND APPEARANCE

PDI SANI HANDS 
instant hand sanitizing wipes cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10819-3918
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10819-3918-1	20 in 1 CELLO PACK	04/01/2016
1		4.15 mL in 1 APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/01/2016

Labeler - Professional Disposables International Inc (800777117)

Registrant - Professional Disposables International Inc (800777117)