FDA.reportPublic FDA data

PURE X Alcohol Wipes

Manufacturer
QUANZHOU AIWINA HYGIENE PRODUCTS CO.,LTD
Effective date
2021-02-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:38:22

Label at a glance#

ProductPURE X Alcohol Wipes
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without rinse. Children under six years of age should be supervised when using this product.

Storage and handling

Store in a dry place away from fire.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Indication and usage

INDICATIONS & USAGE SECTION

  • For hand washing in order to sanitize skin  (hands must air dry)

Warnings

WARNINGS SECTION

  • For external use only.
  • Keep out of reach of eyes. If contact occurs, rinse thoroughly with water.
  • Do not use if you are allergic to any of the ingredients.
  • Discontinue use if irritation or redness develops, and if condition persists for more than 72 hours consult a physician.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep out of reach of children unless under adult supervision.
  • If swallowed, get medical help.

Directions of use

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product and allow to dry without rinse.
  • Children under six years of age should be supervised when using this product.

Other Information

STORAGE AND HANDLING SECTION

  • Store in a dry place away from fire.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

  • Purified (RO) Water, Aloe Vera Extract

SPL UNCLASSIFIED SECTION

KILLS GERMS AND BACTERIA

ETHYL ALCOHOL 75%

Convenient and Easy Cleaning

Simple Application, Dries Quickly

DAILY CLEANING

DEIONIZED WATER

EXQUISITE NON WOVEN FABRIC

DISTRIBUTED BY:

Mansoc Corporation

91-16 25th Avenue

East Elmhurst, NY 11369

Keep out of reach of Children

Made in China

Sanitize your hands every time!

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

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
80671-002-102023-01-30C16284748780-1f386c64a-41f4-0266-e053-dadaa90a7c1aPURE X ® Alcohol Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80671-002-10PURE X Alcohol Wipes3.72 mL in 1 PACKAGECLOTH3.721
80671-002-10PURE X Alcohol Wipes100 in 1 CANISTERCLOTH1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80671-002PURE X ALCOHOL WIPES (ETHYL ALCOHOL) CLOTH [QUANZHOU AIWINA HYGIENE PRODUCTS CO.,LTD]1Legacy NDC, 2 package rows20210221_f2c9bc95-a182-4b9a-a739-cba10c7e6949.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80671-00280671-002-10

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
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT

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
8d6a863f-6e56-4733-a825-62ef8d9b95ecf2c9bc95-a182-4b9a-a739-cba10c7e69492021-02-12WarningsExact identifier
spl id: 8d6a863f-6e56-4733-a825-62ef8d9b95ec
spl set id: f2c9bc95-a182-4b9a-a739-cba10c7e6949

Reported adverse events (FAERS/openFDA)#

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