Disinfectant Spray

Manufacturer
Guangzhou Zhongkebaishi Health Industry CO., LTD
Effective date
2020-07-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:20:26

Label at a glance#

ProductDisinfectant
Active ingredientALCOHOL
Label structure12 sections

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.

Storage and handling

● Store between 15-30°C (59-86°F). ● Avoid freezing and excessive heat above 40°C (104°F).

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

Hand Sanitizer to help reduce bacteria on skin

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame.

Do not use

OTC - DO NOT USE SECTION

● on children less than 2 months of age
● on open skin wounds

When using this product

OTC - WHEN USING SECTION

keep out of eyes, ears, and mouth. If contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation occurs. This may be sign of serious condition.

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

● 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.

Other information

STORAGE AND HANDLING SECTION

● Store between 15-30°C (59-86°F).
● Avoid freezing and excessive heat above 40°C (104°F).

Inactive ingredients

INACTIVE INGREDIENT SECTION

water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

30 mL NDC: 73813-2013-1

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
73813-201373813-2013-1

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
bae23bc3-7c2d-469a-e053-2a95a90a1a64ab21ae3d-83a5-8d7e-e053-2a95a90a53bf2021-02-09WarningsExact identifier
spl set id: ab21ae3d-83a5-8d7e-e053-2a95a90a53bf

Reported adverse events (FAERS/openFDA)#

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