Sanitizer Hand Spray

Manufacturer
MINGSHI TECHNOLOGY CO., LTD | SALES AND PRODUCT SOLUTIONS
Effective date
2021-12-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:25:02

Label at a glance#

ProductSanitizer Hand
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

To help reduce bacteria on the skin when soap and water are unavailable.

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethanol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

To help reduce bacteria on the skin when soap and water are unavailable.

Warnings

WARNINGS SECTION

For External Use only. FLAMMABLE. Keep away from heat or flame

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center immediately

Do not use

OTC - DO NOT USE SECTION

Do not use with children less than 2 months of age

Supervise children under 6 years of age when using this product to avoid swallowing or getting in eyes and on face.

Do not use in open wounds or broken skin.

When using this product

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water

Other Information

OTHER SAFETY INFORMATION

Store between 59-86F (15-30C). -Avoid freezing and temperatures above 104 F (40C).

Sanitizer Hand Spray

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73992-109-052021-12-02C16284748780-1c7ccaba7-2235-fd44-e053-dadaa90aa01bSanitizer Hand Spray
73992-109-052021-07-23C16284748780-1c7ccaba7-2235-fd44-e053-dadaa90aa01bSanitizer Hand Spray

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73992-10973992-109-05

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
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT

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
eff4bfab-5a3f-7429-e053-2995a90ae93aa7aa2bfe-f24e-57ac-e053-2a95a90a148c2022-12-16WarningsExact identifier
spl set id: a7aa2bfe-f24e-57ac-e053-2a95a90a148c

Reported adverse events (FAERS/openFDA)#

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