FDA.reportPublic FDA data

Hand Wipes

Manufacturer
Hannaford Brothers Company | Rockline Industries
Effective date
2020-10-08
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:12:28

Label at a glance#

ProductHand Wipes antibacterial
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Indications and uses

For handwashing to decrease bacteria on the skin

Dosage and administration

​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.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.115%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

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

When using this product

OTC - WHEN USING SECTION

if eye contact occurs, rinse eyes thoroughly with water

Stop use and ask a doctor

OTC - STOP USE SECTION

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

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • ​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

INACTIVE INGREDIENT SECTION

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

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
41268-60041268-600-40

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
DISODIUM COCOAMPHODIACETATE18L9G3U51MIACT
ALCOHOL3K9958V90MIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
EDETATE SODIUMMP1J8420LUIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
ALOE VERA LEAFZY81Z83H0XIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

Source Document#

Source XML · Source PDF

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
ce2ddc1f-c507-99db-e053-2995a90a237b60e006e4-8582-0def-e053-2a91aa0a50292021-10-12WarningsExact identifier
spl set id: 60e006e4-8582-0def-e053-2a91aa0a5029

Reported adverse events (FAERS/openFDA)#

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