FDA.reportPublic FDA data

Wetex Alcohol Prep Pad

Manufacturer
Wetex Inc
Effective date
2022-07-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:50:06

Label at a glance#

ProductWetex Alcohol Prep Pad
Active ingredientISOPROPYL ALCOHOL
Label structure11 sections

Indications and uses

For preparation of the skin prior to an injection

Dosage and administration

Wipe topically and discard after use.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70%......................Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For preparation of the skin prior to an injection

Warnings

WARNINGS SECTION

  • For external use only.
  • Flammable, keep away from fire or flame.

Do not use

OTC - DO NOT USE SECTION

  • Do not use with electrocautery procedures.
  • Do not use in the eyes. If contact occurs, flush eyes with water.

Stop use

OTC - STOP USE SECTION

  • Stop use if irritation and redness develop.If condition persists consult your health care parctitioner.

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

Directions

DOSAGE & ADMINISTRATION SECTION

Wipe topically and discard after use.

Other information

OTHER SAFETY INFORMATION

Store at room temperature 15ºC - 30ºC (59ºF-86ºF)

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Purified Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

82826-001-01 Inner

WETEX

MEDICAL PRODUCTS

ALCOHOL PREP PAD

1 PC

FOR EXTERNAL USE ONLY

SATURED WITH 70% V/V ISOPROPYL ALCOHOL

InnerInner

82826-001-01 Outer

WETEX

MEDICAL PRODUCTS

ALCOHOL PREP PAD

SATURED WITH 70% V/V ISOPROPYL ALCOHOL

FOR EXTERNAL USE ONLY

200 PCS

OuterOuter

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
797544isopropyl alcohol 70 % Medicated PadPSN1
797544isopropyl alcohol 0.7 ML/ML Medicated PadSCD1
797544isopropyl alcohol 70 % Medicated PadSY1
797544isopropyl alcohol 70 % Topical ClothSY1
797544isopropyl alcohol 70 % Topical SwabSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82826-001-012024-01-30C16284748780-10191ceaa-6774-198a-e063-dbdaa90aec3eWetex Alcohol Prep Pad
82826-001-012023-12-13C16284748780-10191ceaa-6774-198a-e063-dbdaa90aec3eWetex Alcohol Prep Pad
82826-001-012023-07-28C16284748780-10191ceaa-6774-198a-e063-dbdaa90aec3eWetex Alcohol Prep Pad

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82826-001-01Wetex Alcohol Prep Pad200 in 1 BOXCLOTH2001
82826-001-01Wetex Alcohol Prep Pad1 in 1 POUCHCLOTH11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82826-001WETEX ALCOHOL PREP PAD (ISOPROPYL ALCOHOL) CLOTH [WETEX INC]1Legacy NDC, 2 package rows20220709_e2b7fd4b-53ae-2fd8-e053-2a95a90a7c73.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
82826-00182826-001-01
78149-003

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
ISOPROPYL ALCOHOLND2M416302ACTIB
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
e2b7fc9d-adcd-578c-e053-2995a90af141e2b7fd4b-53ae-2fd8-e053-2a95a90a7c732022-07-05WarningsExact identifier
spl id: e2b7fc9d-adcd-578c-e053-2995a90af141
spl set id: e2b7fd4b-53ae-2fd8-e053-2a95a90a7c73

Reported adverse events (FAERS/openFDA)#

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