FDA.reportPublic FDA data

Sanitizing Wipes

Manufacturer
Condor Co., Ltd.
Effective date
2020-08-25
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:31:32

Label at a glance#

ProductSanitizing Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure13 sections

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.1%

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin.

For use when soap and water are not available.

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

OTC - DO NOT USE SECTION

in children less than 2 months of age
on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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 right away.

DOSAGE & ADMINISTRATION SECTION

Open packet, remove and unfold pre-moistened tissue. Wipe hands or affected area thoroughly, then discard properly after use. Reseal back after use to keep wipes fresh.

STORAGE AND HANDLING SECTION

Store between 15-30C (59-86F)
Avoid freezing and excessive heat above 40C (104F)

INACTIVE INGREDIENT SECTION

Phenoxy Ethanol, Polyhexamethylene Biguanide Hydrochloride, Purified Water, Propylene Glycol, Ethyl Alcohol, Vitamin E, Lemon Terpenes, Aloe Vera Extract.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

10 wipes NDC: 80144-001-01

10 wipes label10 wipes label

35 wipes NDC: 80144-001-02

35 wipes label35 wipes label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038856benzalkonium Cl 0.1 % Medicated PadPSN4
1038856benzalkonium chloride 1 MG/ML Medicated PadSCD4
1038856benzalkonium chloride 0.1 % Medicated WipesSY4
1038856benzalkonium chloride 0.1 % Topical SwabSY4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80144-001-012023-01-30C16284748780-1f386c64a-1b76-0266-e053-dadaa90a7c1aSanitizing Wipes
80144-001-022023-01-30C16284748780-1f386c64a-1b76-0266-e053-dadaa90a7c1aSanitizing Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80144-001-01Sanitizing Wipes10 mg in 1 POUCHCLOTH104
80144-001-02Sanitizing Wipes35 mg in 1 BOTTLE, PLASTICCLOTH354

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80144-001SANITIZING WIPES (ALCOHOL) CLOTH [CONDOR CO., LTD.]4Legacy NDC, 2 package rows20201014_ad328c9a-e213-6944-e053-2995a90adfff.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80144-00180144-001-01, 80144-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
ALPHA-TOCOPHEROLH4N855PNZ1IACT
POLIHEXANIDE HYDROCHLORIDE4XI6112496IACT
ALCOHOL3K9958V90MIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
LEMON TERPENES5DHA4TVW63IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
PHENOXYETHANOLHIE492ZZ3TIACT

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
adae29dc-9fea-681e-e053-2a95a90a8a4aad328c9a-e213-6944-e053-2995a90adfff2020-08-25WarningsExact identifier
spl id: adae29dc-9fea-681e-e053-2a95a90a8a4a
spl set id: ad328c9a-e213-6944-e053-2995a90adfff

Reported adverse events (FAERS/openFDA)#

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