WeClean Hand Sanitizer Cranberry Spice Scent

Manufacturer
Landy International
Effective date
2022-03-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:05:32

Label at a glance#

ProductWeClean Hand Sanitizer Cranberry Spice Scent
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age When using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

helps eliminate bacteria on hands

Warnings

WARNINGS SECTION

For external use only.
Flammable, Keep away from heat or flame,
Do not use
On children less than 2 months of age. on open skin wounds
When using this product keep out of eyes, ear, and mouth.
In case of contact with eve, rinse eyes thouroughly with water
Stop use and ask a doctor if irritation or rash occurs,
These may be a sign of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. except under adult supervision.

If swallowed, get medical help or contact a poison control center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product on hands to cover all surfaces.
Rub hands together until dry.
Supervise children under 6 years of age When using this product
to avoid swallowing.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Triethanolamine, Water(Aqua), Zea mays(Corn) starch.
Acrylates/C10-0 alkyl acrylate crosspolymer,Chromium Oxide Greens((l 77288),
Fragrance (Parfum),Glycerin,Hydroxypropyl methylcellulose,Mannitol,
Microcrystalline cellulose,Red 33(CI/17200), Red 4(CI14700), Sucrose,

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51706-94651706-946-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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
23ccd184-b260-e4c8-e063-6394a90a3f48aec29870-48e1-1003-e053-2a95a90ac0342024-10-06WarningsExact identifier
spl set id: aec29870-48e1-1003-e053-2a95a90ac034

Reported adverse events (FAERS/openFDA)#

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