FDA.reportPublic FDA data

TION HAND SANITIZER

Manufacturer
WHAIN COSMETIC
Effective date
2020-04-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:06:22

Label at a glance#

ProductTION HAND SANITIZER
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

Uses: Disinfection of hands and skin

Dosage and administration

Directions: ■ place enough product in your palms ■ rub hands together until dry

Label contents#

Full prescribing information#

Active Ingredients 

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: ALCOHOL 70.0%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients:

Water, Sodium Hyaluronate,Butylene Glycol,Camellia Sinensis Leaf Extract,Artemisia Princeps Extract

Purpose

OTC - PURPOSE SECTION

Purpose: SANITIZER

Warnings

WARNINGS SECTION

Warnings:

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

KEEP OUT OF REACH OF CHILDREN

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.

Uses

INDICATIONS & USAGE SECTION

Uses:

Disinfection of hands and skin

Directions

DOSAGE & ADMINISTRATION SECTION

Directions:

■ place enough product in your palms
■ rub hands together until dry

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottleImage of bottle

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73823-050-012023-01-30C16284748780-1f386c649-fb18-0266-e053-dadaa90a7c1abb52c179-8ca9-4333-8401-975598ee55d5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73823-050-01TION HAND SANITIZER100 mL in 1 BOTTLE, SPRAYSPRAY1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73823-050TION HAND SANITIZER (ALCOHOL) SPRAY [WHAIN COSMETIC]1Legacy NDC, 1 package rows20200415_bb52c179-8ca9-4333-8401-975598ee55d5.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73823-05073823-050-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
Water059QF0KO0RIACT
HYALURONATE SODIUMYSE9PPT4THIACT
Butylene Glycol3XUS85K0RAIACT
GREEN TEA LEAFW2ZU1RY8B0IACT

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
b8ca3103-1f62-4dbe-89cc-d2092e0589f8bb52c179-8ca9-4333-8401-975598ee55d52020-04-15WarningsExact identifier
spl id: b8ca3103-1f62-4dbe-89cc-d2092e0589f8
spl set id: bb52c179-8ca9-4333-8401-975598ee55d5

Reported adverse events (FAERS/openFDA)#

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