PyurX

Manufacturer
Novara LLC | NanTong Guarder Medical Technology Co.,Ltd.
Effective date
2021-02-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:37:54

Label at a glance#

ProductPyurX
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry. Children under 6 years of age should be supervised when using this product.

Storage and handling

Store at below or below 75F (24C). May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

75% Alcohol Disinfectant Wet Wipes. 50 count

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizing

Use

INDICATIONS & USAGE SECTION

  • For hand sanitizing to decrease bacteria on skin.
  • Recommened for repeated use.

Warnings

WARNINGS SECTION

  • Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.
  • Do not use on children less than 2 months of age.
  • For external use only.
  • Flammable Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

  • Do not use in the eyes. In case of contact, rinse thoroughly with water.
  • Do not use on children less than 2 months of age.

OTC - STOP USE SECTION

  • Stop use and ask a doctor if irritation or redness develop and persist for more than 72 hours.
  • Swallowed, get medical help or contact a poison control center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

  • Children must be supervised when using this product.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product and allow to dry.
  • Children under 6 years of age should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

  • Store at below or below 75F (24C).
  • May discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

glycerin, Aqua(water), Vitamin E, Aloe

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

frontfront

BackBack

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1307051ethanol 75 % Medicated PadPSN2
1307051ethanol 0.75 ML/ML Medicated PadSCD2
1307051ethanol 75 % Hand Sanitizer WipesSY2
1307051ethyl alcohol 75 % Topical ClothSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80527-351-512022-07-29C16284748780-1e4f33bdf-b3b7-d8a0-e053-dadaa90a6e4eaff3ff26-050a-7f27-e053-2995a90aa09c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80527-351-51PyurX50 mL in 1 PACKAGECLOTH502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80527-351PYURX (DISINFECTANT WET WIPES) CLOTH [NOVARA LLC]2Legacy NDC, 1 package rows20210209_aff3ff26-050a-7f27-e053-2995a90aa09c.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
80527-35180527-351-51

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

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
bad7d195-4bed-7e8c-e053-2995a90aa880aff3ff26-050a-7f27-e053-2995a90aa09c2021-02-08WarningsExact identifier
spl id: bad7d195-4bed-7e8c-e053-2995a90aa880
spl set id: aff3ff26-050a-7f27-e053-2995a90aa09c

Reported adverse events (FAERS/openFDA)#

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