FDA.reportPublic FDA data

Wish Ultra hand sanitizer

Manufacturer
Click Products LLC
Effective date
2020-06-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:16:11

Label at a glance#

ProductWish Ultra hand sanitizer 01
Active ingredientALCOHOL
Label structure9 sections

Label contents#

Full prescribing information#

Hand Sanitizer

DESCRIPTION SECTION

Kills 99.9% of germs

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient Purpose

Ethyl Alcohol 75% v/v Antimicrobial

use

OTC - PURPOSE SECTION

Reduce bacteria and viruses onthe hands that may cause disease.

Warning

WARNINGS SECTION

for external use only.

Flammable

WARNINGS SECTION

Keep away from heat and flame.

When using this product

OTC - WHEN USING SECTION

Avoid contact with face, eyes and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

Stop and ask a doctor if

OTC - STOP USE SECTION

irritation or redness develops.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed get immediate medical help or contact a poison contaol center right away.

INDICATIONS & USAGE SECTION

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and rub into skin until dry.

USER SAFETY WARNINGS SECTION

Children under 6 years of age should be supervised by an adult when using.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water( aqua), Glycerin, Propylene Glycol, Carbomer, Triethanolamine, Fragrance, Aloe Barbadensis( Aloe Vera) Gel, Tocopheryl acetate( vitamin E).

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

54304-040-0154304-040-0154304-040-0254304-040-02

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71611-040-012022-01-28C16284748780-1d6a99b39-b66d-a426-e053-dadaa90af4c2hand sanitizer -60250/ 60260
71611-040-022022-01-28C16284748780-1d6a99b39-b66d-a426-e053-dadaa90af4c2hand sanitizer -60250/ 60260

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71611-040-01Wish Ultra hand sanitizer01222 mL in 1 BOTTLE, PLASTICLIQUID2221
71611-040-02Wish Ultra hand sanitizer011000 mL in 1 BOTTLE, PLASTICLIQUID10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71611-040WISH ULTRA HAND SANITIZER 01 (ALCOHOL) LIQUID [CLICK PRODUCTS LLC]1Legacy NDC, 2 package rows20200605_aca3ca16-c3a9-4a37-b530-e46b3969a521.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71611-04071611-040-01, 71611-040-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOMER 9404Q93RCW27EIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
TROLAMINE9O3K93S3TKIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
COCONUT OILQ9L0O73W7LIACT
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
a74c1432-81e2-35f6-e053-2995a90a7a5eaca3ca16-c3a9-4a37-b530-e46b3969a5212020-06-04WarningsExact identifier
spl id: a74c1432-81e2-35f6-e053-2995a90a7a5e
spl set id: aca3ca16-c3a9-4a37-b530-e46b3969a521

Reported adverse events (FAERS/openFDA)#

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