FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Jiangsu Ouyali Daily Cosmetic Co., Ltd. | WESSCO International
Effective date
2020-10-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:09:58

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Squeeze a significant amount in your palm and rub hands until fully dry. Rinse free.

Storage and handling

Store below 110 °F（43° C).

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v.

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce germs on the skin.

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: avoid contact with eyes. lf contact occurs, rinse thoroughly with water.

OTC - STOP USE SECTION

Stop using and ask a doctor if irritation or redness develops and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children: ln case of accidental ingestion, get medical help or contact a poison control center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Squeeze a significant amount in your palm and rub hands until fully dry.
  • Rinse free.

Other information

STORAGE AND HANDLING SECTION

  • Store below 110 °F（43° C).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl propanol, Aloe Barbadensis leaf Juice, Denatonium benzoate, Fragrance, Glycerin, Maltodextrin, Propylene Glycol, Tocopheryl Acetate, Water.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

29 mL NDC: 76719-015-01 29ml label_129ml label_1 29ml label_229ml label_2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76719-015-012024-12-03C16284748780-1d6a99b39-fe0a-a426-e053-dadaa90af4c2Jiangsu Ouyali Daily Cosmetic Co., Ltd. Hand Sanitizer 29ml 76719-015-01
76719-015-012022-01-28C16284748780-1d6a99b39-fe0a-a426-e053-dadaa90af4c2Jiangsu Ouyali Daily Cosmetic Co., Ltd. Hand Sanitizer 29ml 76719-015-01

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76719-01576719-015-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
MALTODEXTRIN7CVR7L4A2DIACT
ALOE VERA LEAFZY81Z83H0XIACT
CARBOMER INTERPOLYMER TYPE A (55000 CPS)59TL3WG5COIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
WATER059QF0KO0RIACT
DENATONIUM BENZOATE4YK5Z54AT2IACT
AMINOMETHYLPROPANOLLU49E6626QIACT
FRAGRANCE LAVENDER & CHIA F-153480SXS9CO2TZKIACT
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
285eabfc-8e04-0799-e063-6394a90a82bdb294dacc-5ab1-3a29-e053-2a95a90aea9f2024-12-03WarningsExact identifier
spl set id: b294dacc-5ab1-3a29-e053-2a95a90aea9f

Reported adverse events (FAERS/openFDA)#

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