Wish Hand Sanitizing Wipes

Manufacturer
CLICK PRODUCTS LLC
Effective date
2020-09-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:28:43

Label at a glance#

ProductWish Hand Sanitizing Wipes
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping

Storage and handling

/

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only
Do not use in the eyes

Do not use

OTC - DO NOT USE SECTION

  • Do not use in the eyes

OTC - WHEN USING SECTION

/

OTC - STOP USE SECTION

irritation and redness develop
condition persists for 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.

Directions

DOSAGE & ADMINISTRATION SECTION

wet hands thoroughly with product and allow to dry without wiping

Other information

STORAGE AND HANDLING SECTION

/

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Aloe vera leaf juice, Tocopheryl acetate

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71611-063-00Wish Hand Sanitizing Wipes100 in 1 BAGCLOTH1001
71611-063-16Wish Hand Sanitizing Wipes160 in 1 BAGCLOTH1601
71611-063-40Wish Hand Sanitizing Wipes40 in 1 BAGCLOTH401
71611-063-80Wish Hand Sanitizing Wipes80 in 1 BAGCLOTH801

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71611-063WISH HAND SANITIZING WIPES (ETHYL ALCOHOL WIPES) CLOTH [CLICK PRODUCTS LLC]1Legacy NDC, 4 package rows20200908_aec19918-a56f-8876-e053-2a95a90a6ac6.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
71611-06371611-063-40, 71611-063-00, 71611-063-80, 71611-063-16

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
aec19918-a570-8876-e053-2a95a90a6ac6aec19918-a56f-8876-e053-2a95a90a6ac62020-09-07WarningsExact identifier
spl id: aec19918-a570-8876-e053-2a95a90a6ac6
spl set id: aec19918-a56f-8876-e053-2a95a90a6ac6

Reported adverse events (FAERS/openFDA)#

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