Hand Sanitizer Spray

Manufacturer
Meixin Beauty & Health Care Products Co., Ltd.
Effective date
2020-07-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:19:57

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Put enough product on palm and rub hands until drya Children under 6 years of age should be supervised while using this product

Storage and handling

/

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Warnings

WARNINGS SECTION

For external use only. Only on hands
Flammable, keep away from fire or flam

Do not use

OTC - DO NOT USE SECTION

Do not use in or near eyes In case of contact
rinse thoroughly with water

OTC - WHEN USING SECTION

/

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness
develop and 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

Put enough product on palm and rub hands until drya
Children under 6 years of age should be supervised while using this

product

Other information

STORAGE AND HANDLING SECTION

/

Inactive ingredients

INACTIVE INGREDIENT SECTION

Auqa(water), glycerin, parfum

INDICATIONS & USAGE SECTION

To decrease bacteria on skin without soap or water
Recommended for repeated use

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

59159159359360605959592592

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2286295ethanol 75 % Topical SprayPSN2
2286295ethanol 0.75 ML/ML Topical SpraySCD2
2286295ethanol 75 % Topical SpraySY2

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78565-002-01Hand Sanitizer59 mL in 1 BOTTLESPRAY592
78565-002-02Hand Sanitizer59 mL in 1 BOTTLESPRAY592
78565-002-03Hand Sanitizer59 mL in 1 BOTTLESPRAY592
78565-002-04Hand Sanitizer60 mL in 1 BOTTLESPRAY602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78565-002HAND SANITIZER SPRAY [MEIXIN BEAUTY & HEALTH CARE PRODUCTS CO., LTD.]2Legacy NDC, 4 package rows20200703_a8beb06b-b9f1-491c-e053-2995a90ac2bb.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78565-00278565-002-02, 78565-002-01, 78565-002-03, 78565-002-04

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
METHYL BENZOATE6618K1VJ9TIACT
GLYCERINPDC6A3C0OXIACT
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
a970d8b3-ea50-b4c4-e053-2a95a90a91c7a8beb06b-b9f1-491c-e053-2995a90ac2bb2020-07-02WarningsExact identifier
spl id: a970d8b3-ea50-b4c4-e053-2a95a90a91c7
spl set id: a8beb06b-b9f1-491c-e053-2995a90ac2bb

Reported adverse events (FAERS/openFDA)#

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