FDA.reportPublic FDA data

Hand sanitizer

Manufacturer
Yangzhou Lianrun Medical Equipment Co., Ltd.
Effective date
2020-11-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:33:59

Label at a glance#

ProductHand sanitizer
Active ingredientALCOHOL
Label structure10 sections

Dosage and administration

Apply a small amount of product to your palm to cover both hands and rub until dry.

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

  • To decrease bacteris on the skin that potentially can cause disease
  • Recommended for repeated use

Warnings

WARNINGS SECTION

  • Flammable, keep away from heat or flame
  • For external use only
  • Keep out of eyes, ears or mouth. In case of eye contact, flush eyes with water

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develop or if condition persists more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children swallowed, get medical help or contact a Poison Control Center right away. Children should be supervised by an adult when using this product.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply a small amount of product to your palm to cover both hands and rub until dry.

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Vera Leaf, Alpha-Tocopherol Acetate, Carbomer Interpolymer Type A, Aloe(fragrance), Glycerin, Maltodextrin, Propylene Glycol, Water, Aminomethyl Propanol.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

118 mL NDC: 93782-002-01 118mL label118mL label

500 mL NDC: 93782-002-02 500mL label500mL label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN1
1305100ethanol 0.75 ML/ML Topical GelSCD1
1305100ethanol 75 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
93782-002-012022-01-28C16284748780-1d6a99b39-e69d-a426-e053-dadaa90af4c2Yangzhou Lianrun Medical Equipment Co., Ltd. Hand sanitizer 118ml 93782-002-01 500ml 93782-002-02
93782-002-022022-01-28C16284748780-1d6a99b39-e69d-a426-e053-dadaa90af4c2Yangzhou Lianrun Medical Equipment Co., Ltd. Hand sanitizer 118ml 93782-002-01 500ml 93782-002-02

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
93782-002-01Hand sanitizer118 mL in 1 BOTTLEGEL1181
93782-002-02Hand sanitizer500 mL in 1 BOTTLEGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
93782-002HAND SANITIZER GEL [YANGZHOU LIANRUN MEDICAL EQUIPMENT CO., LTD.]1Legacy NDC, 2 package rows20201120_b4740f8e-cddb-58bf-e053-2a95a90a9be3.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
93782-00293782-002-01, 93782-002-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
AMINOMETHYLPROPANOLLU49E6626QIACT
CARBOMER COPOLYMER TYPE A71DD5V995LIACT
ALOEV5VD430YW9IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
GLYCERINPDC6A3C0OXIACT
MALTODEXTRIN7CVR7L4A2DIACT
WATER059QF0KO0RIACT
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
b4742768-693b-5d9e-e053-2a95a90ab8eab4740f8e-cddb-58bf-e053-2a95a90a9be32020-11-19WarningsExact identifier
spl id: b4742768-693b-5d9e-e053-2a95a90ab8ea
spl set id: b4740f8e-cddb-58bf-e053-2a95a90a9be3

Reported adverse events (FAERS/openFDA)#

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