FDA.reportPublic FDA data

Hand Sanitizing Wipes

Manufacturer
Bar-D Company | Zhejiang Qimei Commodity Co.,Ltd.
Effective date
2022-11-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:51:35

Label at a glance#

ProductHand Sanitizing Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

For hand sanitizing to decrase germs on skin.

Dosage and administration

Peel back front sticker and remove wipe(s). Reseal pouch by pressing sticker back in place. Rub all surfaces of hands thoroughly with wipe. Allow hands to dry without additional wiping. Dispose of wipe in trash or compost. Do not flush.

Storage and handling

Store in a cool dry place. Keep closed tightly to retain moisture.

Label contents#

Full prescribing information#

Directions

DOSAGE & ADMINISTRATION SECTION

  • Peel back front sticker and remove wipe(s). Reseal pouch by pressing sticker back in place.
  • Rub all surfaces of hands thoroughly with wipe. Allow hands to dry without additional wiping.
  • Dispose of wipe in trash or compost. Do not flush.

Warnings

WARNINGS SECTION

  • For external use only.
  • Avoid contact with eyes. If contact occurs, flush eyes with water.
  • Stop use and ask a doctor if irritation or redness develops and persists for more than 72 hours.
  • Keep out of reach of children. If swallowed, get medical help or contact a poison control center immediately

Uses

INDICATIONS & USAGE SECTION

For hand sanitizing to decrase germs on skin.

Keep out of reach of children. If swallowed, get medical help or contact a poison control center immediately.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a poison control center immediately.

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose: Antimicrobial

Directions

OTC - STOP USE SECTION

Stop use and ask doctor if irritation or redness develops and persists for more than 72 hours.

Other Information

STORAGE AND HANDLING SECTION

  • Store in a cool dry place.
  • Keep closed tightly to retain moisture.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Propylene Glycol, Glycerin, Phenoxyethanol, Potassium Sorbate, Disodium Cocoamphodiacetate, PEG-40 Hydrogenated Castor Oil, Aloe Vera Extract (Aloe Barbadensis), Tea Tree Oil (Melaleuca Alternifolia Leaf), Chamomile Extract (Chamomilla Recutita), Tocopheryl Acetate (Vitamin E), Peppermint Oil (Mentha Piperita), Citric Acid, Trisodium EDTA

Hand Sanitizing Wipes

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL


Box LabelBox LabelPouch (Bag) LabelPouch (Bag) Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038558benzalkonium chloride 0.13 % Medicated PadPSN2
1038558benzalkonium chloride 1.3 MG/ML Medicated PadSCD2
1038558benzalkonium chloride 0.13 % Topical ClothSY2
1038558benzalkonium chloride 0.13 % Topical SwabSY2
1038558benzalkonium chloride 0.13 GM per 100 GM Topical PadSY2
1038558benzalkonium chloride 0.13 GM per 100 GM Topical SwabSY2
1038558benzalkonium chloride 1 ML per 750 ML Topical SwabSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82303-001-022024-01-30C16284748780-11030e365-45ee-111a-e063-dadaa90a10e2d00e7b2d-0129-68ff-e053-2995a90a339d

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82303-001-01Hand Sanitizing Wipes10 mL in 1 BAGCLOTH102
82303-001-02Hand Sanitizing Wipes6 in 1 BOXCLOTH62

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82303-001HAND SANITIZING WIPES (BENZALKONIUM CHLORIDE (0.13%)) CLOTH [BAR-D COMPANY]2Legacy NDC, 2 package rows20221117_d00e7b2d-0129-68ff-e053-2995a90a339d.zip

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82303-00182303-001-01, 82303-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
GLYCERINPDC6A3C0OXIACT
TEA TREE OILVIF565UC2GIACT
WATER059QF0KO0RIACT
DISODIUM COCOAMPHODIACETATE18L9G3U51MIACT
PEPPERMINT OILAV092KU4JHIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ALOE VERA LEAFZY81Z83H0XIACT
PHENOXYETHANOLHIE492ZZ3TIACT
CHAMOMILEFGL3685T2XIACT
EDETATE TRISODIUM420IP921MBIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
ed9a3485-2f13-64fb-e053-2995a90ad17dd00e7b2d-0129-68ff-e053-2995a90a339d2022-11-16WarningsExact identifier
spl id: ed9a3485-2f13-64fb-e053-2995a90ad17d
spl set id: d00e7b2d-0129-68ff-e053-2995a90a339d

Reported adverse events (FAERS/openFDA)#

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