Yangxiang, Hand Sanitizer, 75% Alcohol, Gel, xxx mL

Manufacturer
Zhejiang Yangxiang Technology Co., Ltd | A03 Lab of BTS
Effective date
2020-05-23
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 23:29:22

Label at a glance#

ProductInstant Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Put enough product on your palm to cover hands and rub hands together briskly until dry. Children under 6 years of age should be supervised when using this product.

Storage and handling

Store at a cool place, avoid sunlight.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Hand sanitizer to help decrease bacteria skin.

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on skin.

Warnings

WARNINGS SECTION

Flammable, Keep away from fire or flame.
For external use only.

Do not use

OTC - DO NOT USE SECTION

When using this product do not use in or near the eyes.

In case of contact, rinse eyes thoroughly with water.

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.

OTC - STOP USE SECTION

Stop using if skin allergles occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

If swallowed, get medical help or contact poisions control center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Put enough product on your palm to cover hands and rub hands together briskly until dry.

Children under 6 years of age should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

Store at a cool place, avoid sunlight.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua (water), Glycerin, Carbomer, Triethanolamine, Vitamin E extract.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

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
75589-10175589-101-25, 75589-101-01, 75589-101-03, 75589-101-15

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Source Document#

Source XML · Source PDF

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
c30f15e0-075b-6ce3-e053-2a95a90a0339a4fde18a-20e6-a866-e053-2a95a90a59f62021-05-24WarningsExact identifier
spl set id: a4fde18a-20e6-a866-e053-2a95a90a59f6

Reported adverse events (FAERS/openFDA)#

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