WET NAPS ANTIBACTERIAL HAND WIPES FRESH- antibacterial hand wipes swab

Wet Naps Antibacterial Hand Wipes by

Drug Labeling and Warnings

Wet Naps Antibacterial Hand Wipes 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

Antiseptic handwash

Use

For hand washing to decrease bacteria on the skin.

Warnings

For external use only.

Do not use in the eyes.

Discontinue use if irritation and redness develop. If condition persists for more than 72 hours consult a doctor.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Directions for container:

• To dispense, lift cover, remove seal, pull center sheet from roll, twist to a point, feed through dispenser hole in cover. Keep lid closed to prevent moisture loss.
• Use as part of your hand cleaning routine.
• Run product onto hands and allow to dry.
• Discard after single use.

Directions for packets or flowrap: see on container the directions to retreive the wipe.

Inactive ingredients

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

Principal Display panel

Wet Naps

Antibacterial Hand Wipes

Moisturizes with Aloe

Kills 99.99% of Germs

Fresh Scent

Front Canister:

Back Canister:

Packet:

Box:

flowrap:

Bonus 30ct box:

Bonus 54ct canister:

INGREDIENTS AND APPEARANCE

WET NAPS ANTIBACTERIAL HAND WIPES  FRESH
antibacterial hand wipes swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10819-7011
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
ALCOHOL (UNII: 3K9958V90M)
SORBIC ACID (UNII: X045WJ989B)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PPG-2 HYDROXYETHYL COCAMIDE (UNII: 34N07GUJ3X)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10819-7011-1	193.1 mL in 1 CANISTER; Type 0: Not a Combination Product	01/01/2014
2	NDC: 10819-7011-2	24 in 1 BOX	03/01/2014
2		4.4 mL in 1 PACKET; Type 0: Not a Combination Product
3	NDC: 10819-7011-3	20 in 1 CELLO PACK	01/01/2016
3		2.6 mL in 1 APPLICATOR; Type 0: Not a Combination Product
4	NDC: 10819-7011-4	30 in 1 BOX	08/01/2016
4		4.4 mL in 1 PACKET; Type 0: Not a Combination Product
5	NDC: 10819-7011-5	266 mL in 1 CANISTER; Type 0: Not a Combination Product	08/01/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/01/2014

Labeler - Professional Disposables International Inc. (800777117)

Registrant - Professional Disposables International Inc. (800777117)