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]

ACTIVE INGREDIENT

Active ingredient

Benzalkonium chloride 0.13%

PURPOSE

Purpose

Antibacterial

INDICATIONS & USAGE

Uses · to decrease bacteria on the skin

· recommended for repeated use

WARNINGS

Warnings

For external use only

WHEN USING

When using this product keep away from eyes.

In case of eye contact, rinses eyes with water.

STOP USE

Stop use and ask a doctor if irritation or redness

develop or last more than 72 hours.

KEEP OUT OF REACH OF CHILDREN

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

help or contact a Poison Control Center immediately.

DOSAGE & ADMINISTRATION

Directions

· rub wipe thoroughly over all surfaces of both hands

· allow to dry without wiping

· supervise children under 6 years old

· not recommended for infants

· dispose of wipe in trash; do not flush

INACTIVE INGREDIENT

Inactive ingredients

Water, Alcohol Denat., Phenoxyethanol, PEG-8 Dimethicone, Caprylyl Glycol, Dihydroxypropyl PEG-5 Linoleammonium Chloride, Potassium Sorbate, Disodium EDTA, Citric Acid, Fragrance, Aloe Barbadensis Leaf Juice

PRINCIPAL DISPLAY PANEL

1 Wipe
5.0 IN × 7.8 IN
(12.7 cm × 19.8 cm)
NDC: 11822-0286-1

24 Wipes
Individually Wrapped
5.0 IN × 7.8 IN
(12.7 cm × 19.8 cm)
NDC: 11822-0286-2

PRINCIPAL DISPLAY PANEL

40 Wipes
5.7 IN × 7.5 IN
(14.5 cm × 19.05 cm)
NDC: 11822-0286-3

INGREDIENTS AND APPEARANCE

SIMPLIFY ANTIBACTERIAL HAND WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11822-0286
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 g

Inactive Ingredients
Ingredient Name	Strength
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ALCOHOL (UNII: 3K9958V90M)
PEG-8 DIMETHICONE (UNII: GIA7T764OD)
EDETATE DISODIUM (UNII: 7FLD91C86K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11822-0286-2	24 in 1 BOX	07/01/2024
1	NDC: 11822-0286-1	1 in 1 POUCH
1		0.00425 g in 1 PATCH; Type 0: Not a Combination Product
2	NDC: 11822-0286-3	40 in 1 CANISTER	07/01/2024
2		0.00429 g in 1 PATCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	07/01/2024

Labeler - RITE AID CORPORATION (014578892)