FDA.reportPublic FDA data

Disinfectant Spray

Manufacturer
Guangzhou Zhongkebaishi Health Industry CO., LTD
Effective date
2020-07-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:21:04

Label at a glance#

ProductDisinfectant
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Spray a one to three times into palm of hand Rub thoroughly over all surfaces of both hands Rub hands together briskly until dry Other, Spray a one to three times to where want

Storage and handling

Keep away from the direct sunlight Store at room temperature

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand sanitizing to decrease bacteria on the skin

Recommended for repeated use

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 years of age
  • on open skin wounds or if allergy to alcohol

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops or if condition persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Spray a one to three times into palm of hand

Rub thoroughly over all surfaces of both hands

Rub hands together briskly until dry

Other, Spray a one to three times to where want

Other information

STORAGE AND HANDLING SECTION

Keep away from the direct sunlight

Store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

30 mL NDC: 73813-2012-1

PDPPDP

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73813-201273813-2012-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
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
bae24636-b3ff-ef90-e053-2995a90aa36eaaab68e6-73f7-44b0-e053-2995a90a52d32021-02-09WarningsExact identifier
spl set id: aaab68e6-73f7-44b0-e053-2995a90a52d3

Reported adverse events (FAERS/openFDA)#

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