FDA.reportPublic FDA data

Alcohol Wipes

Manufacturer
Hangzhou Lookon Commodity Co., Ltd.
Effective date
2022-10-18
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:51:06

Label at a glance#

ProductAlcohol Wipes
Active ingredientALCOHOL
Label structure14 sections

Storage and handling

Note: Do not store above 100℉. Non-staining may discolor some fabrics.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Ethyl Alcohol 70% v/v

OTC - PURPOSE SECTION

Purpose:Antiseptic

INDICATIONS & USAGE SECTION

Uses: to decrease bacteria on the skin

WARNINGS SECTION

Warnings:

For external use only

Flammable: Keep away from flame or high heat.

When use this product avoid contact with the eyes,face and broken skin.

Stop use and ask a doctor if irritation or redness develop or last more than 72 hours.

Keep out of reach of children. If swallowed,get medical help or contact a Poison Control Center right away.

OTC - WHEN USING SECTION

When use this product avoid contact with the eyes,face and broken skin.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develop or last more than 72 hours.

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.

STORAGE AND HANDLING SECTION

Note: Do not store above 100℉. Non-staining may discolor some fabrics.

DOSAGE & ADMINISTRATION SECTION

Directions:

Rub wipe thoroughly over all surfaces of both hands

Allow to dry without wiping

Supervise children under 6 years old

Not recommended for infants

Dispose of wipes in trash after use. Do not flush.

INACTIVE INGREDIENT SECTION

Inactive Ingredient:

Aqua,Glycerin, Propylene Glycol, Aloe Barbadensis Leaf Juice, Decyl Glucoside

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC：74835-012-01

250 in pail250 in pail

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC：74835-012-02

1000 in pail1000 in pail

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC：74835-012-03

1200 in bag1200 in bag

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 74835-012-04

50 in bag label50 in bag label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1489307ethanol 70 % Medicated PadPSN3
1489307ethanol 0.7 ML/ML Medicated PadSCD3
1489307ethanol 70 % Medicated PadSY3
1489307ethanol 70 % Medicated WipesSY3
1489307ethyl alcohol 70 % ClothSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74835-012-012024-01-30C16284748780-11030e365-6744-111a-e063-dadaa90a10e2Alcohol Wipes
74835-012-022024-01-30C16284748780-11030e365-6744-111a-e063-dadaa90a10e2Alcohol Wipes
74835-012-032024-01-30C16284748780-11030e365-6744-111a-e063-dadaa90a10e2Alcohol Wipes
74835-012-042024-01-30C16284748780-11030e365-6744-111a-e063-dadaa90a10e2Alcohol Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74835-012-01Alcohol Wipes250 in 1 PAILCLOTH2503
74835-012-01Alcohol Wipes0.68 mL in 1 PATCHCLOTH0.683
74835-012-02Alcohol Wipes0.68 mL in 1 PATCHCLOTH0.683
74835-012-02Alcohol Wipes1000 in 1 PAILCLOTH10003
74835-012-03Alcohol Wipes1200 in 1 BAGCLOTH12003
74835-012-03Alcohol Wipes0.68 mL in 1 PATCHCLOTH0.683
74835-012-04Alcohol Wipes50 in 1 BAGCLOTH503
74835-012-04Alcohol Wipes0.68 mL in 1 PATCHCLOTH0.683

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74835-012ALCOHOL WIPES CLOTH [HANGZHOU LOOKON COMMODITY CO., LTD.]3Legacy NDC, 8 package rows20221020_e6e27f81-89a8-1486-e053-2995a90a4d8a.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74835-01274835-012-01, 74835-012-02, 74835-012-03, 74835-012-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ALOE VERA LEAFZY81Z83H0XIACT
DECYL GLUCOSIDEZ17H97EA6YIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
eb5a9658-5bb2-93a4-e053-2995a90a613de6e27f81-89a8-1486-e053-2995a90a4d8a2022-10-18WarningsExact identifier
spl id: eb5a9658-5bb2-93a4-e053-2995a90a613d
spl set id: e6e27f81-89a8-1486-e053-2995a90a4d8a

Reported adverse events (FAERS/openFDA)#

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