Germ smash hand sanitizer

Manufacturer
Zhejiang Meizhiyuan Cosmetics Co., Ltd | Townley Inc.
Effective date
2020-05-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:28:39

Label at a glance#

ProductGerm smash hand sanitizer 01
Active ingredientALCOHOL
Label structure14 sections

Label contents#

Full prescribing information#

HAND SANITIZER

DESCRIPTION SECTION

Non-sterile solution

Kills 99.99% of germs

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient Purpose

Ethyl Alcohol 80% v/v Antimicrobial

Use(s)

OTC - PURPOSE SECTION

Hand sanitizer to help reduce bacterial potentially can cause disease.

For use when soap and water not available.

Warning

WARNINGS SECTION

For external use only.

Flammable, Keep away from heat and flame.

Do not use

OTC - DO NOT USE SECTION

In Children less than 2months of age

on open skin wounds

WHEN USING THIS PRODUCT

OTC - WHEN USING SECTION

Keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes throughly with water.

OTC - STOP USE SECTION

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

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed get immediate medical, get medical help or contact a poison control center right away.

INDICATIONS & USAGE SECTION

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product on hands to cover all surfaces. Rub hands together until dry.

USER SAFETY WARNINGS SECTION

supervise children under 6 years of age when using this product to avoid swallowing.

Other information

OTHER SAFETY INFORMATION

Store between 15-30 oC (59-86 oF)

Avoid freezing and excessive heat above 40 oC (104 oF)

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

purified water USP, glycerin, Hydrogen peroxide.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

54304-071-0154304-071-01

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54304-07154304-071-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

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.

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
aa779706-0baf-4c27-e053-2a95a90a8d05a6b3301f-cc91-ca8b-e053-2995a90a8a302020-07-15WarningsExact identifier
spl set id: a6b3301f-cc91-ca8b-e053-2995a90a8a30

Reported adverse events (FAERS/openFDA)#

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