WET NAPS ANTIBACTERIAL HAND WIPES- 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 Westrock Rkt Company, WESTROCK RKT COMPANY. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Warning section

For external use only. Keep out of reach of children. If swallowed get medical help or contact a posion control center right away. Do not use in eyes. Discontinue use if irritation develop. If condition persists for more than 72 hours consult a doctor.

INACTIVE INGREDIENT

Purified water, SD alcohol 40, Sorbic Acid, PPG-2 Hydroxyethyl Cocamide, Disodium EDTA, Aloe Barbadensis leaf join, Fragrance

Directions

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

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

PURPOSE

Antiseptic handwash

ACTIVE INGREDIENT

Benzalkonium chloride 0.13% mg/ml

DOSAGE & ADMINISTRATION

Strength Benzalkonium chloride 0.13% mg/ml

Cloth wipe administraion

handwipe.jpg

Consumer facing image of hand wipes.

INGREDIENTS AND APPEARANCE

WET NAPS ANTIBACTERIAL HAND WIPES 
antibacterial hand wipes swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71928-7011(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)
PPG-2 HYDROXYETHYL COCAMIDE (UNII: 34N07GUJ3X)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71928-7011-1	193 mL in 1 CANISTER; Type 0: Not a Combination Product	01/01/2014

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

Labeler - Westrock Rkt Company (603215539)

Establishment
Name	Address	ID/FEI	Business Operations
WESTROCK RKT COMPANY		603215539	relabel(71928-7011) , repack(71928-7011)