FDA.reportPublic FDA data

HAND SANITIZER

Manufacturer
Taizhou Huangyan Delishi Daily Necessity Co., Ltd.
Effective date
2020-07-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:20:42

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Wet hands thoroughly with product. briskly rub hands together until dry. Supervise children under 6 years in the use of this product.

Storage and handling

Store at 20°C to 25°C (68°to 77°F ) May discolor certain fabrics.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from fire and flame.

Do not use in the eyes. Incase of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or redness develops and persists for more than 72 hours.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Do not use

OTC - DO NOT USE SECTION

Do not use in the eyes. Incase of contact, rinse eyes thoroughly with water.

OTC - WHEN USING SECTION

For external use only. Flammable. Keep away from fire and flame.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops and 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. briskly rub hands together until dry.

Supervise children under 6 years in the use of this product.

Other information

STORAGE AND HANDLING SECTION

Store at 20°C to 25°C (68°to 77°F )

May discolor certain fabrics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Glycerin, Carbomer, Triethanolamine, Propylene Glycol, Aloe Barbadensis Leaf Juice.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

6060.

500500

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN1
581660ethanol 0.62 ML/ML Topical GelSCD1
581660ethanol 62 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76681-002-012021-07-23C16284748780-1c7ccaba7-2037-fd44-e053-dadaa90aa01bHAND SANITIZER
76681-002-022021-07-23C16284748780-1c7ccaba7-2037-fd44-e053-dadaa90aa01bHAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76681-002-01HAND SANITIZER60 mL in 1 BOTTLEGEL601
76681-002-02HAND SANITIZER500 mL in 1 BOTTLEGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76681-002HAND SANITIZER GEL [TAIZHOU HUANGYAN DELISHI DAILY NECESSITY CO., LTD.]1Legacy NDC, 2 package rows20200709_a9fa6ebf-e44d-39d8-e053-2995a90aacba.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76681-00276681-002-02, 76681-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT
TRIETHANOLAMINE DODECYLBENZENESULFONATE8HM7ZD48HNIACT
CARBOMER 934Z135WT9208IACT

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
a9fa68ac-3144-6080-e053-2a95a90a4efca9fa6ebf-e44d-39d8-e053-2995a90aacba2020-07-08WarningsExact identifier
spl id: a9fa68ac-3144-6080-e053-2a95a90a4efc
spl set id: a9fa6ebf-e44d-39d8-e053-2995a90aacba

Reported adverse events (FAERS/openFDA)#

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