FDA.reportPublic FDA data

Simplify Antibacterial Hand

Manufacturer
Rite Aid Corporation
Effective date
2025-12-16
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 01:26:00

Label at a glance#

ProductSimplify Antibacterial Hand Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Dosage and administration

wipe hands thoroughly with product and allow to dry for children under 6, use only under adult supervision not recommended for infants

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only-hands

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

medical help or contact a Poison Control Center right away.

SPL UNCLASSIFIED SECTION

When using this product

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

thoroughly with water.

  • avoid contact with broken skin

SPL UNCLASSIFIED SECTION

Stop use and ask a doctor if

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

SPL UNCLASSIFIED SECTION

Drug Facts (continued)

Directions

DOSAGE & ADMINISTRATION SECTION

  • wipe hands thoroughly with product and

allow to dry

  • for children under 6, use only under adult

supervision

  • not recommended for infants

Inactive Ingredients

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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)

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.

Wipes front panelWipes front panel

Wipes front graphicsWipes front graphics

Wipes drug factsWipes drug facts

Wipes front graphics moreWipes front graphics more

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038558benzalkonium chloride 0.13 % Medicated PadPSN8
1038558benzalkonium chloride 1.3 MG/ML Medicated PadSCD8
1038558benzalkonium chloride 0.13 % Topical ClothSY8
1038558benzalkonium chloride 0.13 % Topical SwabSY8
1038558benzalkonium chloride 0.13 GM per 100 GM Topical PadSY8
1038558benzalkonium chloride 0.13 GM per 100 GM Topical SwabSY8
1038558benzalkonium chloride 1 ML per 750 ML Topical SwabSY8

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130011822219150GTIN-13: 0011822219150
EAN-13: 0011822219150
GTIN-12: 011822219150
UPC-A: 011822219150
GTIN storage (14 digits): 00011822219150		Wipes drug facts more.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11822-0283-1Simplify Antibacterial Hand Wipes20 in 1 POUCHCLOTH208

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11822-028311822-0283-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
POLYSORBATE 207T1F30V5YHIACT
CAPRYLYL/CAPRYL OLIGOGLUCOSIDEE00JL9G9K0IACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
POLYGLYCERYL-6 CAPRYLATEDGV8R54VG7IACT
SODIUM BENZOATEOJ245FE5EUIACT
POLYGLYCERYL-4 LAURATE82V7NG3DYTIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
4618b382-ac24-9e5f-e063-6394a90ad7920286e81d-568c-9cb7-e063-6294a90a24d32025-12-16WarningsExact identifier
spl id: 4618b382-ac24-9e5f-e063-6394a90ad792
spl set id: 0286e81d-568c-9cb7-e063-6294a90a24d3

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.