FDA.reportPublic FDA data

LUOYS Hand Sanitizer

Manufacturer
Zhejiang Yiwu Limei Cosmetics Co., Ltd
Effective date
2020-05-04
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-05-31 23:09:34

Label at a glance#

ProductLUOYS Hand Sanitizer
Active ingredientALCOHOL
Label structure13 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until 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#

SPL UNCLASSIFIED SECTION

NA

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

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

  • Place enough product on hands to cover all surfaces. Rub hands together until 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, propylene glycol, glycerin, carbomer, triethanolamine

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

29 mL NDC: 74765-008-01

50 mL NDC: 74765-008-02

60 mL NDC: 74765-008-03

80 mL NDC: 74765-008-04

100 mL NDC: 74765-008-05

236 mL NDC: 74765-008-06

300 mL NDC: 74765-008-07

500 mL NDC: 74765-008-08 500ml label500ml label

1000 mL NDC: 74765-008-09

2000 mL NDC: 74765-008-10

3000 mL NDC: 74765-008-11

5000 mL NDC: 74765-008-12

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN8
581662ethanol 0.7 ML/ML Topical GelSCD8
581662ethanol 70 % Topical GelSY8
581662ethyl alcohol 70 % Topical GelSY8

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74765-008-012022-01-28C16284748780-1d6a99b39-a596-a426-e053-dadaa90af4c2a4ce58ac-3217-5f83-e053-2a95a90a27b7
74765-008-022022-01-28C16284748780-1d6a99b39-a596-a426-e053-dadaa90af4c2a4ce58ac-3217-5f83-e053-2a95a90a27b7
74765-008-032022-01-28C16284748780-1d6a99b39-a596-a426-e053-dadaa90af4c2a4ce58ac-3217-5f83-e053-2a95a90a27b7
74765-008-042022-01-28C16284748780-1d6a99b39-a596-a426-e053-dadaa90af4c2a4ce58ac-3217-5f83-e053-2a95a90a27b7
74765-008-052022-01-28C16284748780-1d6a99b39-a596-a426-e053-dadaa90af4c2a4ce58ac-3217-5f83-e053-2a95a90a27b7
74765-008-062022-01-28C16284748780-1d6a99b39-a596-a426-e053-dadaa90af4c2a4ce58ac-3217-5f83-e053-2a95a90a27b7
74765-008-072022-01-28C16284748780-1d6a99b39-a596-a426-e053-dadaa90af4c2a4ce58ac-3217-5f83-e053-2a95a90a27b7
74765-008-082022-01-28C16284748780-1d6a99b39-a596-a426-e053-dadaa90af4c2a4ce58ac-3217-5f83-e053-2a95a90a27b7
74765-008-092022-01-28C16284748780-1d6a99b39-a596-a426-e053-dadaa90af4c2a4ce58ac-3217-5f83-e053-2a95a90a27b7
74765-008-102022-01-28C16284748780-1d6a99b39-a596-a426-e053-dadaa90af4c2a4ce58ac-3217-5f83-e053-2a95a90a27b7
74765-008-112022-01-28C16284748780-1d6a99b39-a596-a426-e053-dadaa90af4c2a4ce58ac-3217-5f83-e053-2a95a90a27b7
74765-008-122022-01-28C16284748780-1d6a99b39-a596-a426-e053-dadaa90af4c2a4ce58ac-3217-5f83-e053-2a95a90a27b7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74765-008-01LUOYS Hand Sanitizer29 mL in 1 BOTTLEGEL298
74765-008-02LUOYS Hand Sanitizer50 mL in 1 BOTTLEGEL508
74765-008-03LUOYS Hand Sanitizer60 mL in 1 BOTTLEGEL608
74765-008-04LUOYS Hand Sanitizer80 mL in 1 TUBEGEL808
74765-008-05LUOYS Hand Sanitizer100 mL in 1 BOTTLEGEL1008
74765-008-06LUOYS Hand Sanitizer236 mL in 1 BOTTLEGEL2368
74765-008-07LUOYS Hand Sanitizer300 mL in 1 BOTTLEGEL3008
74765-008-08LUOYS Hand Sanitizer500 mL in 1 BOTTLEGEL5008
74765-008-09LUOYS Hand Sanitizer1000 mL in 1 BOTTLEGEL10008
74765-008-10LUOYS Hand Sanitizer2000 mL in 1 BOTTLEGEL20008
74765-008-11LUOYS Hand Sanitizer3000 mL in 1 BOTTLEGEL30008
74765-008-12LUOYS Hand Sanitizer5000 mL in 1 BOTTLEGEL50008

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74765-008LUOYS HAND SANITIZER (ALCOHOL) GEL [ZHEJIANG YIWU LIMEI COSMETICS CO., LTD]8Legacy NDC, 12 package rows20200505_a4ce58ac-3217-5f83-e053-2a95a90a27b7.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74765-00874765-008-01, 74765-008-02, 74765-008-03, 74765-008-04, 74765-008-05, 74765-008-06, 74765-008-07, 74765-008-08, 74765-008-09, 74765-008-10, 74765-008-11, 74765-008-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOMER 9804Q93RCW27EIACT
GLYCERINPDC6A3C0OXIACT
TROLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
PROPYLENE GLYCOL6DC9Q167V3IACT

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
a4ce581b-828a-0a39-e053-2995a90a1c50a4ce58ac-3217-5f83-e053-2a95a90a27b72020-05-04WarningsExact identifier
spl id: a4ce581b-828a-0a39-e053-2995a90a1c50
spl set id: a4ce58ac-3217-5f83-e053-2a95a90a27b7

Reported adverse events (FAERS/openFDA)#

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