alcohol wipes

Manufacturer
Zhejiang quercus daily necessities Co., Ltd
Effective date
2020-08-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:23:56

Label at a glance#

Productalcohol wipes
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Lift inner seal sticker and remove wipe. Gently wipe face and hand to clean. After use, reseal the sticker to prevent the wipes from drying out.

Storage and handling

Store at a shady, cool and dry place Avoid direct sunlight and open flames Wipes are insoluble in water. Please do not throw into toilet.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

to decrease bacterial on the skin that could cause disease

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

  • if you are allergic to any of the ingredients
  • on children less than 2 years of aga unless directed by a doctor

When using this product

OTC - WHEN USING SECTION

Avoid contact with eyes and damaged skin. In case of eye contact, flush eyes with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if signs of irritation or rash appear

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

Lift inner seal sticker and remove wipe. Gently wipe face and hand to clean. After use, reseal the sticker to prevent the wipes from drying out.

Other information

STORAGE AND HANDLING SECTION

  • Store at a shady, cool and dry place
  • Avoid direct sunlight and open flames
  • Wipes are insoluble in water. Please do not throw into toilet.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1 PCS NDC 90017-002-01 OAK ALCOHOLOAK ALCOHOL

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
90017-002-012022-01-28C16284748780-1d6a99b39-780a-a426-e053-dadaa90af4c275% alcohol wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
90017-002-01alcohol wipes1 in 1 POUCHCLOTH11
90017-002-01alcohol wipes6.5 g in 1 APPLICATORCLOTH6.51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
90017-002ALCOHOL WIPES (ALCOHOL) CLOTH [ZHEJIANG QUERCUS DAILY NECESSITIES CO., LTD]1Legacy NDC, 2 package rows20200806_ac2fc6a1-844f-56aa-e053-2995a90abfea.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
90017-00290017-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
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
ac2fc6a1-8450-56aa-e053-2995a90abfeaac2fc6a1-844f-56aa-e053-2995a90abfea2020-08-05WarningsExact identifier
spl id: ac2fc6a1-8450-56aa-e053-2995a90abfea
spl set id: ac2fc6a1-844f-56aa-e053-2995a90abfea

Reported adverse events (FAERS/openFDA)#

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