HAND WIPES ANTIBACTERIAL- benzalkonium chloride cloth

Hand Wipes by

Drug Labeling and Warnings

Hand Wipes by is a Otc medication manufactured, distributed, or labeled by Hannaford Brothers Company, Rockline Industries. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.115%

Purpose

Antibacterial

Uses

For handwashing to decrease bacteria on the skin

Warnings

For external use only

Do not use

• in the eyes
• ​if you are allergic to any of the ingredients

When using this product

if eye contact occurs, rinse eyes thoroughly with water

Stop use and ask a doctor

if irritation and redness develop and persist for more than 72 hours

Keep out of reach of children

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

Directions

• ​Storage. Store at room temperature
• Dispensing. Remove seal band. Lift tab at front of lid. Pull up corner of center sheet and thread through dispenser slit in lid. Close lid to retain moisture
• Use. Apply wipe thouroughly to hands as desired. Allow to dry without wiping.
• Disposal. Dispose of used wipes in trash recepacle after use. Do not flush.

Inactive Ingredients

Water, Aloe Barbadensis Leaf Extract, Disodium Cocoamphodiacetate, SD Alcohol 40-B, Methylchloroisothiazolinine, Methylisothiazolinone, Tocopheryl Acetate, Disodium EDTA, Citric acid, Fragrance

Package Label

INGREDIENTS AND APPEARANCE

HAND WIPES  ANTIBACTERIAL
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 41268-600
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.115 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
ALCOHOL (UNII: 3K9958V90M)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
EDETATE SODIUM (UNII: MP1J8420LU)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 41268-600-40	40 in 1 PACKAGE; Type 0: Not a Combination Product	12/01/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	12/01/2017

Labeler - Hannaford Brothers Company (006949556)

Registrant - Rockline Industries (966920881)