LECHAT Sanitizer Gel New 60% Ethanol

Manufacturer
Mega Creation Inc.
Effective date
2021-11-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:44:53

Label at a glance#

ProductLECHAT
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Wet hands thoroughly with the product and rub into the skin till dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 60% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

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. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a 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

  • Wet hands thoroughly with the product and rub into the skin till dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified Water, IsopiopylAlcohol, Hydrogen Peroxide, Glycerin, Isopropyl Myristate, Acrylates/C10-30 Ally Acrylate Crosspolymer, Aminomethyl Propanol, Cocoyl Caprylocaprate, Aloe Barbadensis Leaf Extract, Tocopheryl-acetate, fragrance, Lavender Oil, Orange Oil, Grapefruit Oil

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

51 mL NDC: 77857-832-0151 mL NDC: 77857-832-0151 mL NDC: 77857-832-01

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581658ethanol 60 % Topical GelPSN2
581658ethanol 0.6 ML/ML Topical GelSCD2
581658ethanol 60 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77857-832-01LECHAT51 mL in 1 BOTTLEGEL512
77857-832-16LECHAT473 mL in 1 BOTTLEGEL4732
77857-832-32LECHAT946 mL in 1 BOTTLEGEL9462

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77857-832LECHAT (HAND SANITIZER GEL) GEL [MEGA CREATION INC.]2Legacy NDC, 3 package rows20211112_c4f6c403-2fea-5bf0-e053-2995a90a0b0f.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77857-83277857-832-01, 77857-832-16, 77857-832-32

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 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
d07898db-bdea-83de-e053-2995a90aeb14c4f6c403-2fea-5bf0-e053-2995a90a0b0f2021-11-10WarningsExact identifier
spl id: d07898db-bdea-83de-e053-2995a90aeb14
spl set id: c4f6c403-2fea-5bf0-e053-2995a90a0b0f

Reported adverse events (FAERS/openFDA)#

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