FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Zhejiang USHAS Cosmetics Co.,Ltd
Effective date
2020-07-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:21:37

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

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

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#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75%v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

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 fire 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

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may by signs of a serious condition.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Posion 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

Water,

glycerin,

acrylates/vinyl isodecanoate crosspolymer,

aminomethyl propanol,

fragrance,

panthenol,

aloe barbadensis leaf juice,

tocopheryl acetate

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73962-00673962-006-01, 73962-006-02, 73962-006-03, 73962-006-04, 73962-006-05, 73962-006-06, 73962-006-07, 73962-006-08, 73962-006-09, 73962-006-10, 73962-006-11, 73962-006-12, 73962-006-13, 73962-006-14, 73962-006-15, 73962-006-16, 73962-006-17, 73962-006-18, 73962-006-19, 73962-006-20, 73962-006-21, 73962-006-22, 73962-006-23, 73962-006-24, 73962-006-25, 73962-006-26, 73962-006-27, 73962-006-28, 73962-006-29, 73962-006-30, 73962-006-31, 73962-006-32, 73962-006-33, 73962-006-34, 73962-006-35, 73962-006-36, 73962-006-37, 73962-006-38, 73962-006-39, 73962-006-40, 73962-006-41, 73962-006-42, 73962-006-43, 73962-006-44, 73962-006-45, 73962-006-46, 73962-006-47, 73962-006-48, 73962-006-49, 73962-006-50, 73962-006-51, 73962-006-52, 73962-006-53, 73962-006-54, 73962-006-55, 73962-006-56, 73962-006-57, 73962-006-58, 73962-006-59, 73962-006-60, 73962-006-61, 73962-006-62, 73962-006-63, 73962-006-64, 73962-006-65, 73962-006-66, 73962-006-67, 73962-006-68, 73962-006-69, 73962-006-70, 73962-006-71

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
PANTHENOLWV9CM0O67ZIACT
CARBOMER COPOLYMER TYPE A71DD5V995LIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT

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
d07398bb-a479-0bcf-e053-2995a90a2e8aaa5f47ba-3a09-7275-e053-2a95a90a70bb2021-11-10WarningsExact identifier
spl set id: aa5f47ba-3a09-7275-e053-2a95a90a70bb

Reported adverse events (FAERS/openFDA)#

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