HAND SANITIZER PREMIUM FORMULA

Manufacturer
LTP Global | ICOMAX Co., Ltd.
Effective date
2020-06-08
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:16:30

Label at a glance#

ProductHAND SANITIZER PREMIUM FORMULA
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping for children under 6, use only under adult supervision not recommened for infacts

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

  • to decrease bacteria that potentially can cause disease
  • recommended for repeated use

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 and redness develop
  • condition persists for more than 72 hours

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
  • for children under 6, use only under adult supervision
  • not recommened for infacts

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)
  • 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

30mL Box30mL Box30mL Label30mL Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN4
581662ethanol 0.7 ML/ML Topical GelSCD4
581662ethanol 70 % Topical GelSY4
581662ethyl alcohol 70 % Topical GelSY4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73812-002-042022-01-28C16284748780-1d6a99b39-a8ab-a426-e053-dadaa90af4c2a60e10c4-3b8a-60a1-e053-2a95a90ab8a9

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73812-002-03HAND SANITIZER PREMIUM FORMULA30 mL in 1 POUCHGEL304
73812-002-04HAND SANITIZER PREMIUM FORMULA20 in 1 BOXGEL204

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73812-002HAND SANITIZER PREMIUM FORMULA (HAND SANITIZER) GEL [LTP GLOBAL]4Legacy NDC, 2 package rows20200609_a60e10c4-3b8a-60a1-e053-2a95a90ab8a9.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
73812-00273812-002-03, 73812-002-04

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
a78c2c44-676b-1521-e053-2995a90a022da60e10c4-3b8a-60a1-e053-2a95a90ab8a92020-06-08WarningsExact identifier
spl id: a78c2c44-676b-1521-e053-2995a90a022d
spl set id: a60e10c4-3b8a-60a1-e053-2a95a90ab8a9

Reported adverse events (FAERS/openFDA)#

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