DISINFECTING WIPES

Manufacturer
Wenzhou Jiajia show Daily Necessities Co., Ltd
Effective date
2021-01-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:36:48

Label at a glance#

ProductDISINFECTING WIPES
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Place a piece of product to rub hands and external skin, if not liquid leak from the wipe, dispose it, and use a new piece. Supervise children under 6 years of age when usingthis product to avoid swallowing.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75%

OTC - PURPOSE SECTION

Antiseptic

Use[s]

INDICATIONS & USAGE SECTION

Hand and skin sanitizer to help reduce bacteriathat potentially can cause disease.For use when soap and water are not available

WARNINGS SECTION

For external use only. Flammalbe. 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 eye, ear and mouth. In case of contact with eyes, rinse eyesthoroughly with water

OTC - ASK DOCTOR 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. lf swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Place a piece of product to rub hands and external skin, if not liquid leak from the wipe, dispose it, and use a new piece.
Supervise children under 6 years of age when usingthis product to avoid swallowing.

HOW SUPPLIED SECTION

Store between 15-30°C(59-86°F)
Avoid freezing and excessive heat above40°C(104°F)

INACTIVE INGREDIENT SECTION

Purified water USP, Didecyldimonium Chloride

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1307051ethanol 75 % Medicated PadPSN1
1307051ethanol 0.75 ML/ML Medicated PadSCD1
1307051ethanol 75 % Hand Sanitizer WipesSY1
1307051ethyl alcohol 75 % Topical ClothSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84287-001-012022-07-29C16284748780-1e4f33bdf-b06a-d8a0-e053-dadaa90a6e4eb8ab7dd3-fd9f-11a2-e053-2a95a90aaa24

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84287-001-01DISINFECTING WIPES4.8 mL in 1 PATCHCLOTH4.81
84287-001-01DISINFECTING WIPES80 in 1 PACKETCLOTH801

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84287-001DISINFECTING WIPES (ALCOHOL) CLOTH [WENZHOU JIAJIA SHOW DAILY NECESSITIES CO., LTD]1Legacy NDC, 2 package rows20210112_b8ab7dd3-fd9f-11a2-e053-2a95a90aaa24.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84287-00184287-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIDECYLDIMONIUM CHLORIDEJXN40O9Y9BIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT

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
b8ab7dd3-fda0-11a2-e053-2a95a90aaa24b8ab7dd3-fd9f-11a2-e053-2a95a90aaa242021-01-11WarningsExact identifier
spl id: b8ab7dd3-fda0-11a2-e053-2a95a90aaa24
spl set id: b8ab7dd3-fd9f-11a2-e053-2a95a90aaa24

Reported adverse events (FAERS/openFDA)#

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