FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Meixin Beauty & Health Care Products Co., Ltd.
Effective date
2020-09-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:28:36

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Put enough product in your palm to cover hands and rubands together brisky until dry. Children under 6 years of age should be supervised when using.

Storage and handling

Store below(43°C)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on skin.

Warnings

WARNINGS SECTION

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

When using this product do not use in or near the eyes.
In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor in case of rash or irritation stop using and ask a doctor.

Keep out of reach of chlldren.if ingested call your doctor or go to the emergency services.

Do not use

OTC - DO NOT USE SECTION

do not use in or near the eyes.

OTC - WHEN USING SECTION

When using this product do not use in or near the eyes.
In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor in case of rash or irritation stop using and ask a doctor.

Keep out of reach of chlldren.if ingested call your doctor or go to the emergency services.

OTC - STOP USE SECTION

Stop use and ask a doctor in case of rash or irritation stop using and ask a doctor.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of chlldren.if ingested call your doctor or go to the emergency services.

Directions

DOSAGE & ADMINISTRATION SECTION

Put enough product in your palm to cover hands and rubands together brisky until dry.
Children under 6 years of age should be supervised when using.

Other information

STORAGE AND HANDLING SECTION

Store below(43°C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Acry-lates/c10-30 Alkyl Acrylate crosspolymer, Triethanolamine,Sargassum Fusiforme Extract,Poterium Sanguisorba Root Extract,Parfum.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

78565-016-01 500ml78565-016-01 500ml

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-136901784991017GTIN-13: 6901784991017
EAN-13: 6901784991017
GTIN storage (14 digits): 06901784991017		78565-016-01 500ml.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78565-016-012022-01-28C16284748780-1d6a99b39-7ae6-a426-e053-dadaa90af4c278565-016 Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78565-016-01Hand Sanitizer500 mL in 1 BOTTLEGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78565-016HAND SANITIZER GEL [MEIXIN BEAUTY & HEALTH CARE PRODUCTS CO., LTD.]1Legacy NDC, 1 package rows20200907_aeb4a0b3-8e42-e471-e053-2995a90a368b.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78565-01678565-016-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
FRAGRANCE CLEAN ORC0600327329LCV5BTFIACT
SARGASSUM FUSIFORMEX436TJ4A11IACT
SANGUISORBA MINOR ROOT11YGU8I0TTIACT
CARBOMER INTERPOLYMER TYPE A (55000 CPS)59TL3WG5COIACT
TROLAMINE9O3K93S3TKIACT

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
aeb49da2-bc1c-e63d-e053-2995a90a965caeb4a0b3-8e42-e471-e053-2995a90a368b2020-09-07WarningsExact identifier
spl id: aeb49da2-bc1c-e63d-e053-2995a90a965c
spl set id: aeb4a0b3-8e42-e471-e053-2995a90a368b

Reported adverse events (FAERS/openFDA)#

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