SIMPLIFY ANTIBACTERIAL HAND WIPES- benzalkonium chloride cloth

Simplify Antibacterial Hand Wipes by

Drug Labeling and Warnings

Simplify Antibacterial Hand Wipes by is a Otc medication manufactured, distributed, or labeled by Rite Aid Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

Active Ingredient

Benzalkonium chloride 0.13%

Purpose

Antiseptic

Use

to decrease bacteria on the skin

Warnings

For external use only-hands

Keep out of the reach of children. If swallowed, get

medical help or contact a Poison Control Center right away.

When using this product

• Keep out of eyes. In case of contact with eyes, flush

thoroughly with water.

• avoid contact with broken skin

Stop use and ask a doctor if

• irritation or redness develops
• condition persists for more than 72 hours

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Drug Facts (continued)

Directions

• wipe hands thoroughly with product and

allow to dry

• for children under 6, use only under adult

supervision

• not recommended for infants

Inactive Ingredients

water (aqua), glycerin, sodium benzoate, potassium sorbate,
aloe barabadensis leaf juice, fragrance (parfum),
caprylyl/capryl glucoside, polyglyceryl-4 laurate/sebacate,
polyglyceryl-6 caprylate/caprate, citric acid, polysorbate 20

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DISTRIBUTED BY: RITE AID,
2.00 NEWBERRY COMMONS, ETTERS. PA 17319
www.riteaid.com

*Testing based on a subset of FDA proposal published June 17, 1994.

20 Wipes 5.5 x 7 in (14 x 17.8 cm)

Simplify ®

Antibacterial

Hand Wipes

Gentle Cleansing

• With aloe
• Scented
• Kills 99.9% of

Most Common Germs*

• Dermatologist Tested

20 Hand Wipes

OPEN

Do Not Flush

5.5 x 7 in (14 x 17.8 cm)

INGREDIENTS AND APPEARANCE

SIMPLIFY ANTIBACTERIAL HAND WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11822-0283
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
POLYSORBATE 20 (UNII: 7T1F30V5YH)
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
POLYGLYCERYL-6 CAPRYLATE (UNII: DGV8R54VG7)
SODIUM BENZOATE (UNII: OJ245FE5EU)
POLYGLYCERYL-4 LAURATE (UNII: 82V7NG3DYT)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11822-0283-1	20 in 1 POUCH; Type 0: Not a Combination Product	09/11/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	09/11/2023

Labeler - Rite Aid Corporation (014578892)