FDA.reportPublic FDA data

LONIMAX Hand Sanitising

Manufacturer
ZHEJIANG SHUNAN INDUSTRY&TRADE CO., LTD
Effective date
2020-05-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:09:26

Label at a glance#

ProductLONIMAX Hand Sanitising
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping

Storage and handling

Store below 105F

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

NA

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% 

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand washing to help decrease bacteria on the skin only when water is not available

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from fire and flame

OTC - WHEN USING SECTION

When using this product do not get into eyes. When contact occurs, rinse eyes thoroughly with water

May discolor fabrics

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develop

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

  • Wet hands thoroughly with product and allow to dry without wiping

Other information

STORAGE AND HANDLING SECTION

  • Store below 105F

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Carbomer, Xanthan Gum, glycerin, Aloe Vera Extract, Allantoin, Vitamin E, Cellulose, Lactose, Jojoba Alcohol, Hyfrogenated

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

cc

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN2
1305100ethanol 0.75 ML/ML Topical GelSCD2
1305100ethanol 75 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75556-001-012022-01-28C16284748780-1d6a99b39-bf23-a426-e053-dadaa90af4c29d6267f2-6914-460f-b87e-c111af46edd6
75556-001-022022-01-28C16284748780-1d6a99b39-bf23-a426-e053-dadaa90af4c29d6267f2-6914-460f-b87e-c111af46edd6
75556-001-032022-01-28C16284748780-1d6a99b39-bf23-a426-e053-dadaa90af4c29d6267f2-6914-460f-b87e-c111af46edd6
75556-001-042022-01-28C16284748780-1d6a99b39-bf23-a426-e053-dadaa90af4c29d6267f2-6914-460f-b87e-c111af46edd6
75556-001-052022-01-28C16284748780-1d6a99b39-bf23-a426-e053-dadaa90af4c29d6267f2-6914-460f-b87e-c111af46edd6

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75556-001-01LONIMAX Hand Sanitising250 mL in 1 BOTTLEGEL2502
75556-001-02LONIMAX Hand Sanitising60 mL in 1 BOTTLEGEL602
75556-001-03LONIMAX Hand Sanitising237 mL in 1 BOTTLEGEL2372
75556-001-04LONIMAX Hand Sanitising500 mL in 1 BOTTLEGEL5002
75556-001-05LONIMAX Hand Sanitising1000 mL in 1 BOTTLEGEL10002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75556-001LONIMAX HAND SANITISING (ALCOHOL) GEL [ZHEJIANG SHUNAN INDUSTRY&TRADE CO., LTD]2Legacy NDC, 5 package rows20200503_9d6267f2-6914-460f-b87e-c111af46edd6.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75556-00175556-001-01, 75556-001-02, 75556-001-03, 75556-001-04, 75556-001-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
XANTHAN GUMTTV12P4NEEIACT
WATER059QF0KO0RIACT
CARBOMER 934Z135WT9208IACT
TOCOPHEROLR0ZB2556P8IACT
ALOE VERA WHOLEKIZ4X2EHYXIACT
ALLANTOIN344S277G0ZIACT
ALPHA CELLULOSEI355QGZ19AIACT
.ALPHA.-LACTOSEMJF4JAT10BIACT
HYDROGENATED JOJOBA OIL7F674YQ5SOIACT
ALCOHOL3K9958V90MACTIB

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
a4b7265a-101b-2697-e053-2995a90aecf49d6267f2-6914-460f-b87e-c111af46edd62020-05-02WarningsExact identifier
spl id: a4b7265a-101b-2697-e053-2995a90aecf4
spl set id: 9d6267f2-6914-460f-b87e-c111af46edd6

Reported adverse events (FAERS/openFDA)#

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