Ushas Antibacterial Hand Sanitizer

Manufacturer: Zhejiang USHAS Cosmetics Co.,Ltd
Effective date: 2020-07-13
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-01 23:21:37

Label at a glance#

ProductUshas Antibacterial Hand Sanitizer

Active ingredientALCOHOL

Label structure8 sections

Dosage and administration

Place enough product in your palm to thoroughly cover your hands. Rub hands together briskly until dry. Children under 8 years old should be supervised when using this product.

Storage and handling

Do not store above 110F (43C). May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

Active purpose ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 72%(v/v)

Purpose

OTC - PURPOSE SECTION

Antiseptic

Features

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin. Recommended for repeated use. Delicate and fast dry. Use anywhere without water.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water( Aqua)

Glycerin,

Aloe Yohyju Matsu Ekisu,

Acrylates/C10-30 Alkyl Acrylate Crosspolymer,

Triethanolamine,

Fragrance(Parfum)

May contain:FD&C Red No.40(CI 16035), FD&C Yellow No.5( 19140), FD&C Blue No.1 (CI 42090), D&C Red No.33 (CI 17200)

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product in your palm to thoroughly cover your hands.
Rub hands together briskly until dry.
Children under 8 years old should be supervised when using this product.

Warining

WARNINGS SECTION

Flammable, keep away from fire or flame.

For external use only.

When using this product

OTC - WHEN USING SECTION

When using this product, do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

If irritation or rash appears and lasts, stop use and ask a doctor.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Posion Conrol Center right away.

Other Information

STORAGE AND HANDLING SECTION

Do not store above 110F (43C).
May discolor certain fabrics or surfaces.

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

Products#

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

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

Ushas Antibacterial Hand Sanitizer
Alcohol
FD&C RED NO. 40
FD&C BLUE NO. 1
D&C RED NO. 33
WATER
CARBOMER COPOLYMER TYPE A
TROLAMINE
GLYCERIN
ALOE
FD&C YELLOW NO. 5

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73962-005	73962-005-01, 73962-005-02, 73962-005-03, 73962-005-04, 73962-005-05, 73962-005-06, 73962-005-07, 73962-005-08, 73962-005-09, 73962-005-10, 73962-005-11, 73962-005-12, 73962-005-13, 73962-005-14, 73962-005-15, 73962-005-16, 73962-005-17, 73962-005-18, 73962-005-19, 73962-005-20, 73962-005-21, 73962-005-22, 73962-005-23, 73962-005-24, 73962-005-25, 73962-005-26, 73962-005-27, 73962-005-28, 73962-005-29, 73962-005-30, 73962-005-31, 73962-005-32, 73962-005-33, 73962-005-34, 73962-005-35, 73962-005-36, 73962-005-37, 73962-005-38, 73962-005-39, 73962-005-40, 73962-005-41, 73962-005-42, 73962-005-43, 73962-005-44, 73962-005-45, 73962-005-46, 73962-005-47, 73962-005-48, 73962-005-49, 73962-005-50, 73962-005-51, 73962-005-52, 73962-005-53, 73962-005-54, 73962-005-55, 73962-005-56, 73962-005-57, 73962-005-58, 73962-005-59, 73962-005-60, 73962-005-61, 73962-005-62, 73962-005-63, 73962-005-64, 73962-005-65, 73962-005-66, 73962-005-67, 73962-005-68, 73962-005-69, 73962-005-70, 73962-005-71

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
Name	UNII	Kind
FD&C RED NO. 40	WZB9127XOA	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT
D&C RED NO. 33	9DBA0SBB0L	IACT
WATER	059QF0KO0R	IACT
CARBOMER COPOLYMER TYPE A	71DD5V995L	IACT
TROLAMINE	9O3K93S3TK	IACT
GLYCERIN	PDC6A3C0OX	IACT
ALOE	V5VD430YW9	IACT
ALCOHOL	3K9958V90M	ACTIB
FD&C YELLOW NO. 5	I753WB2F1M	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
d07395c5-d6e9-70a9-e053-2995a90a36f8			aa4eef74-c87a-1862-e053-2995a90a539e	2021-11-10	Warnings	Exact identifier spl set id: aa4eef74-c87a-1862-e053-2995a90a539e

Reported adverse events (FAERS/openFDA)#

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