FDA.reportPublic FDA data

HAND SANITIZER

Manufacturer
Taizhou Huangyan Delishi Daily Necessity Co., Ltd.
Effective date
2020-06-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:17:06

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure10 sections

Dosage and administration

Place enough product in palm to cover hands and Rub hands together briskly until dry. Children under 6,use only under adult suoervision. Not recommended for infants.

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

To help reduce bacteria and germs on the skin

Do not use

OTC - DO NOT USE SECTION

In children less than 2 month of age. On open skin wounds

OTC - WHEN USING SECTION

/

OTC - STOP USE SECTION

If irritation or rash occurs. These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product in palm to cover hands and Rub hands together briskly until dry.

Children under 6,use only under adult suoervision.

Not recommended for infants.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Carbomer, Glycerol, Triethanolamine(TEA), Fragrance

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

61615252535357576464

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76681-012-012021-07-23C16284748780-1c7ccaba7-2955-fd44-e053-dadaa90aa01bHAND SANITIZER
76681-012-022021-07-23C16284748780-1c7ccaba7-2955-fd44-e053-dadaa90aa01bHAND SANITIZER
76681-012-032021-07-23C16284748780-1c7ccaba7-2955-fd44-e053-dadaa90aa01bHAND SANITIZER
76681-012-042021-07-23C16284748780-1c7ccaba7-2955-fd44-e053-dadaa90aa01bHAND SANITIZER
76681-012-052021-07-23C16284748780-1c7ccaba7-2955-fd44-e053-dadaa90aa01bHAND SANITIZER
76681-012-062021-07-23C16284748780-1c7ccaba7-2955-fd44-e053-dadaa90aa01bHAND SANITIZER
76681-012-072021-07-23C16284748780-1c7ccaba7-2955-fd44-e053-dadaa90aa01bHAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76681-012-01HAND SANITIZER500 mL in 1 BOTTLEGEL5002
76681-012-02HAND SANITIZER237 mL in 1 BOTTLEGEL2372
76681-012-03HAND SANITIZER237 mL in 1 BOTTLEGEL2372
76681-012-04HAND SANITIZER100 mL in 1 BOTTLEGEL1002
76681-012-05HAND SANITIZER60 mL in 1 BOTTLEGEL602
76681-012-06HAND SANITIZER503 mL in 1 BOTTLEGEL5032
76681-012-07HAND SANITIZER59 mL in 1 BOTTLEGEL592

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76681-012HAND SANITIZER GEL [TAIZHOU HUANGYAN DELISHI DAILY NECESSITY CO., LTD.]2Legacy NDC, 7 package rows20200611_a79f29a6-9290-1541-e053-2995a90a28be.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
76681-01276681-012-05, 76681-012-01, 76681-012-03, 76681-012-04, 76681-012-02, 76681-012-06, 76681-012-07

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
FRAGRANCE LAVENDER & CHIA F-153480SXS9CO2TZKIACT
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
a7b72113-d716-5793-e053-2995a90af570a79f29a6-9290-1541-e053-2995a90a28be2020-06-10WarningsExact identifier
spl id: a7b72113-d716-5793-e053-2995a90af570
spl set id: a79f29a6-9290-1541-e053-2995a90a28be

Reported adverse events (FAERS/openFDA)#

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