Wish Ultra Hand Sanitizer A Coconut Kinda Life

Manufacturer
Zhejiang Meizhiyuan Cosmetics Co.,Ltd
Effective date
2022-11-18
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:46:39

Label at a glance#

ProductWish Ultra Hand Sanitizer A Coconut Kinda Life
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

For occasional and personal domestic use. Rub thoroughly into hands for at least 30 seconds. Allow to dry. children should be supervised by an adult when using this product. Apply as needed. Store at room temperature below 110 o F (43 o C)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v.

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on the skin that may cause disease.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat and flame.
When using this product avoid contat with face, eyes and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.
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.

Directions

DOSAGE & ADMINISTRATION SECTION

For occasional and personal domestic use. Rub thoroughly into hands for at least 30 seconds. Allow to dry. children should be supervised by an adult when using this product.

Apply as needed. Store at room temperature below 110 oF (43 oC)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Propylene Glycol, Glycerin,Carbomer, Fragrance, Aminomethyl Propanol, Aloe Barbadensis (Aloe Vera) Gel, Tocopheryl Acetate (Vitamin E, Lactose, Zea Mays corn starch, Sucrose, Microcrystalline cellose, Hydroxylpropyl Methylcellulose, Ultramarines(I77007), Blue No. 1, FD&C Yellow No. 5.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80204-032-012022-03-08C16284748780-1d6a99b39-e270-a426-e053-dadaa90af4c2305f4286-653b-4869-a1df-932b36db4578
80204-032-012022-01-28C16284748780-1d6a99b39-e270-a426-e053-dadaa90af4c2305f4286-653b-4869-a1df-932b36db4578

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80204-03280204-032-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 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
a2892649-2fae-4c85-94c9-96ac1fbd4044305f4286-653b-4869-a1df-932b36db45782022-11-18WarningsExact identifier
spl id: a2892649-2fae-4c85-94c9-96ac1fbd4044
spl set id: 305f4286-653b-4869-a1df-932b36db4578

Reported adverse events (FAERS/openFDA)#

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