FDA.reportPublic FDA data

MHS Moisturizing Hand Sanitizer

Manufacturer
Moisture 22 Co., Ltd
Effective date
2022-12-21
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:43:28

Label at a glance#

ProductMHS Moisturizing Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Dosage and administration

Place a small amount of the product onto the hands and rub hands together to spread evenly.

Storage and handling

Properly stored in a cool, dry area, avoid direct sunlight. Store up to 5 years in a sealed container.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride (0.05%)

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

For hand sanitizing to reduce bacteria on the skin.

Do not use

OTC - DO NOT USE SECTION

If you are allergic to any of the ingredients.

OTC - WHEN USING SECTION

Avoid getting into eyes (if contact occurs, wash well with clean water.

Do not mix with other chemicals.

OTC - STOP USE SECTION

Stop use andconsult 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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Place a small amount of the product onto the hands and rub hands together to spread evenly.

Other information

STORAGE AND HANDLING SECTION

Properly stored in a cool, dry area, avoid direct sunlight. Store up to 5 years in a sealed container.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Thymol, 2-Phenoxyethanol, Water, Glycerol, 1,2-Hexanediol, Aloe Barbadensis Leaf Juice, Chamomile Extract, Allantoin

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front and Back LabelsFront and Back Labels500 mL NDC: 90014-002-02

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
90014-00290014-002-02, 90014-002-01

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
WATER059QF0KO0RIACT
ALLANTOIN344S277G0ZIACT
CHAMOMILEFGL3685T2XIACT
GLYCERINPDC6A3C0OXIACT
HEXANEDIOLZIA319275IIACT
ALOE VERA LEAFZY81Z83H0XIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
THYMOL3J50XA376EIACT
PHENOXYETHANOLHIE492ZZ3TIACT

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
ffa08db7-7365-b8c0-e053-6294a90ad9deabb52a5a-71a8-5757-e053-2995a90af1e92023-07-03WarningsExact identifier
spl set id: abb52a5a-71a8-5757-e053-2995a90af1e9

Reported adverse events (FAERS/openFDA)#

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