SANI PRO SANI-HANDS ANTIBACTERIAL WIPE- antibacterial wipe swab

Sani Pro Sani-Hands Antibacterial Wipe by

Drug Labeling and Warnings

Sani Pro Sani-Hands Antibacterial Wipe 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

Benzalkonium chloride 0.13%w/w

Purpose

Antimicrobial

Use

For hand washing to decrease bacteria on the skin

Warnings

• For external use only.
• If swallowed, get medical help or contact a Poison Control Center right away.
• Do not use in or contact the the eyes.
• Discontiue use if irritation and redness develp. If condition persists for more than 72 hours, consult a doctor

Keep out of reach of children

Directions

• To dispense, lift cover, remove seal, pull center sheet from roll, twist to a point, and feed through dispenser hole in cover. Keep cap closed to prevent moisture loss.
• Use entire wipe to thoroughly wipe hands, fingers and wrists.
• To sanitize, use multiple wipes.
• Discard after single use.

Other information

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

Inactive ingredients

Purified Water, SD Alcohol 40, Sorbic Acid, PPG-2 Hydroxyethyl Cocamide, Disodium EDTA, Aloe Barbadensis Leaf Juice, Fragrance

SPL UNCLASSIFIED SECTION

Professional Disposables International, Inc.

2 Nice-Pak, Orangeburg, NY 10962-1376 - USA - 1866-673-4376

Made in USA with domestic and imported materials

NSF logo

Nonfood Compounds Program Listed E3 Registration ~151433

Principal display panels

Sani Porfessional Brand

Sani-Hands Antibacterial wipes

Kills 99.99% of germs

Hypoallergenic with moisturing aloe

Front label 150 countt canister

Back label 150 count canister

Front label 300 count canister

Back label 300 count canister

INGREDIENTS AND APPEARANCE

SANI PRO SANI-HANDS ANTIBACTERIAL WIPE 
antibacterial wipe swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10819-7014
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
SORBIC ACID (UNII: X045WJ989B)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
EDETATE DISODIUM (UNII: 7FLD91C86K)
PPG-2 HYDROXYETHYL COCAMIDE (UNII: 34N07GUJ3X)
MICROCITRUS AUSTRALIS FRUIT (UNII: 9DNS80T428)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10819-7014-1	300 in 1 CANISTER	10/01/2016
1		2.67 mL in 1 APPLICATOR; Type 0: Not a Combination Product
2	NDC: 10819-7014-2	150 in 1 CANISTER	10/01/2016
2		2.14 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	10/01/2016

Labeler - Professional Disposables International Inc (800777117)

Registrant - Professional Disposables International Inc (800777117)

Establishment
Name	Address	ID/FEI	Business Operations
Professional Disposables International Inc		800777117	manufacture(10819-7014)