HAND SANITIZER PREMIUM FORMULA

Manufacturer
LTP Global | ICOMAX Co., Ltd.
Effective date
2020-06-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:18:38

Label at a glance#

ProductHAND SANITIZER PREMIUM FORMULA
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Put enough product in your palm to cover hands and rub hands together briskly until dry Children under 6 years should be supervised when using this product

Storage and handling

Store between 59-86°F (15-30°C) Avoid freezing and excessive heat above 104°F (40°C) Do not use on children under two months of age.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

  • to decrease bacteria on the skin that could cause disease

Warnings

WARNINGS SECTION

For external use only : hands

Flammable. Keep away from heat or flame.

OTC - WHEN USING SECTION

When using this product

  • keep out of eyes. In case of contact with eyes, flush thoroughly with water.
  • avoid contact with broken skin
  • do not inhale or ingest

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • irritation or rash occurs. These may be signs of serious condition.

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

  • Put enough product in your palm to cover hands and rub hands together briskly until dry
  • Children under 6 years should be supervised when using this product

Other information

STORAGE AND HANDLING SECTION

  • Store between 59-86°F (15-30°C)
  • Avoid freezing and excessive heat above 104°F (40°C)
  • Do not use on children under two months of age.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Carbomer, Trolamine, L-Menthol, Green Tea Leaf, Aloe Vera Leaf

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

POUCH LABELPOUCH LABELOut Box LabelOut Box Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73812-002-052022-01-28C16284748780-1d6a99b39-dbc7-a426-e053-dadaa90af4c2a8a548c0-ac25-430f-e053-2995a90a0400

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73812-002-02HAND SANITIZER PREMIUM FORMULA2 mL in 1 POUCHGEL21
73812-002-05HAND SANITIZER PREMIUM FORMULA100 in 1 BOXGEL1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73812-002HAND SANITIZER PREMIUM FORMULA (HAND SANITIZER) GEL [LTP GLOBAL]1Legacy NDC, 2 package rows20200623_a8a548c0-ac25-430f-e053-2995a90a0400.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73812-00273812-002-02, 73812-002-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
a8a55204-6901-3164-e053-2a95a90a94d5a8a548c0-ac25-430f-e053-2995a90a04002020-06-22WarningsExact identifier
spl id: a8a55204-6901-3164-e053-2a95a90a94d5
spl set id: a8a548c0-ac25-430f-e053-2995a90a0400

Reported adverse events (FAERS/openFDA)#

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