FDA.reportPublic FDA data

WISH HAND SANITIZER PINEAPPLE DREAM

Manufacturer
CLICK PRODUCTS LLC
Effective date
2024-06-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:14:37

Label at a glance#

ProductWISH HAND SANITIZER PINEAPPLE DREAM
Active ingredientALCOHOL
Label structure13 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient:

Ethyl Alcohol 70% v/v

OTC - PURPOSE SECTION

Purpose

Antimicrobial

INDICATIONS & USAGE SECTION

USE: · Hand sanitizer to help reduce bacteria on the skin that may cause disease.

WARNINGS SECTION

Warnings: for external use only.

Flammable. Keep away from heat and flame.

OTC - WHEN USING SECTION

When using this product · avoid contact with face, eyes and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

OTC - STOP USE SECTION

Stop use and ask a doctor if

· irritation or redness develops.

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.

DOSAGE & ADMINISTRATION SECTION

Directions

· spray enough product in your palm to thoroughly cover your hands.

· rub hands together briskly until dry. Recommended for repeated use.

· children under 6years of age should be supervised when using this product.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: · Water(Aqua), Glycerin, Carbomer, Aminomethyl Propanol, Fragrance, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ITEM#60350
Pineapple Dream
1.2 FL OZ. (35ml)
NDC: 71611-091-01

PN 60350 35ml labelPN 60350 35ml label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ITEM#60351
Pineapple Dream
1.2 FL OZ. (35ml)
NDC: 71611-091-02

PD 60351 35ml labelPD 60351 35ml label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ITEM#60352
Pineapple Dream
1.5 FL OZ. (45ml)
NDC: 71611-091-03

PD 60352 45ml labelPD 60352 45ml label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ITEM#60353
Pineapple Dream
1.5 FL OZ. (45ml)
NDC: 71611-091-04

PD 60353 45ml labelPD 60353 45ml label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71611-091-01WISH HAND SANITIZER PINEAPPLE DREAM35 mL in 1 BOTTLEGEL351
71611-091-01WISH HAND SANITIZER PINEAPPLE DREAM1 in 1 BAGGEL11
71611-091-02WISH HAND SANITIZER PINEAPPLE DREAM35 mL in 1 BOTTLEGEL351
71611-091-03WISH HAND SANITIZER PINEAPPLE DREAM45 mL in 1 BOTTLEGEL451
71611-091-03WISH HAND SANITIZER PINEAPPLE DREAM1 in 1 BAGGEL11
71611-091-04WISH HAND SANITIZER PINEAPPLE DREAM45 mL in 1 BOTTLEGEL451

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71611-091WISH HAND SANITIZER PINEAPPLE DREAM (ALCOHOL) GEL [CLICK PRODUCTS LLC]16 package rows20240704_1b9ea84f-df02-fe16-e063-6294a90acb0f.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71611-09171611-091-01, 71611-091-02, 71611-091-03, 71611-091-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
ALCOHOL3K9958V90MACTIB
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
AMINOMETHYLPROPANOLLU49E6626QIACT

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
1b9ea84f-df03-fe16-e063-6294a90acb0f1b9ea84f-df02-fe16-e063-6294a90acb0f2024-06-24WarningsExact identifier
spl id: 1b9ea84f-df03-fe16-e063-6294a90acb0f
spl set id: 1b9ea84f-df02-fe16-e063-6294a90acb0f

Reported adverse events (FAERS/openFDA)#

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