GIANT EAGLE ANTIBACTERIAL HAND WIPES- benzalkonium chloride cloth

Giant Eagle Antibacterial Hand Wipes by

Drug Labeling and Warnings

Giant Eagle Antibacterial Hand Wipes by is a Otc medication manufactured, distributed, or labeled by Giant Eagle. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial

Uses

• for hand sanitizing to decrease bacteria on the skin.
• recommended for repeated use

Warnings

For external use only.

When using this product

avoid contact with eyes. In case of contact, flush eyes with water.

Stop use and ask a doctor

if irritation or redness develops, or if condition persists for more than 72 hours.

Keep out of the reach of children.

If swallowed, get medical help or contact Poison Control Center right away (1-800-222-1222)

Directions

• adults and children 2 years and over: apply to hands; allow to dry without wiping.
• children under 2 years: ask a doctor before use.

Other information

• store at room temperature
• keep closed tightly.
• may discolor certain fabrics or surfaces

Inactive ingredients

Purified Waterr, SD Alcohol 40, Phenoxyethanol, Decyl Glucoside, Potassium Sorbate, Sodium Benzoate, Disodium EDTA, Citric Acid, Aloe Barbadensis (Aloe) Leaf Extract, Fragrance.

Principal Display Panel

giant eagle

Antibacterial

HAND

WIPES

FRESH SCENT

40 WIPES

INGREDIENTS AND APPEARANCE

GIANT EAGLE ANTIBACTERIAL HAND WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 56194-575
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 g  in 100

Inactive Ingredients
Ingredient Name	Strength
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
WATER (UNII: 059QF0KO0R)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
SODIUM BENZOATE (UNII: OJ245FE5EU)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 56194-575-40	40 in 1 PACKAGE; Type 0: Not a Combination Product	06/22/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	06/22/2022

Labeler - Giant Eagle (929989007)