FDA.reportPublic FDA data

81422-009 Hand Sanitizer Spray

Manufacturer
Shenzhen Lynns Industrial Co., Ltd.
Effective date
2021-01-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:37:02

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

·wet hands thoroughly with product and allow to dry without wiping. ·For children under 6, use only under adult supervision.

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

75%ethyl alcohol by volume....antimicrobial

Purpose

OTC - PURPOSE SECTION

antimicrobial

Use

INDICATIONS & USAGE SECTION

Use to help reduce bacterial on skin.

Warnings

WARNINGS SECTION

Flammable.External use only

Do not use on open skin wounds or children under 2 months of age

When using this product avoid contact with eyes.If case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.

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

Do not use

OTC - DO NOT USE SECTION

Do not use on open skin wounds or children under 2 months of age

OTC - WHEN USING SECTION

When using this product avoid contact with eyes.If case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.

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

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash develops and continues 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

·wet hands thoroughly with product and allow to dry without wiping.
·For children under 6, use only under adult supervision.

Other information

STORAGE AND HANDLING SECTION

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

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

81422-009-00--Hand Sanitizer Spray 500ml

81422-009-00--Hand Sanitizer Spray 500ml81422-009-00--Hand Sanitizer Spray 500ml

81422-009-37--Hand Sanitizer Spray 1Gallon

81422-009-37--Hand Sanitizer Spray 1Gallon81422-009-37--Hand Sanitizer Spray 1Gallon

81422-009-50--Hand Sanitizer Spray 50ml

81422-009-50--Hand Sanitizer Spray 50ml81422-009-50--Hand Sanitizer Spray 50ml

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2286295ethanol 75 % Topical SprayPSN1
2286295ethanol 0.75 ML/ML Topical SpraySCD1
2286295ethanol 75 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81422-009-002022-07-29C16284748780-1e4f33bdf-abae-d8a0-e053-dadaa90a6e4e81422-009 Hand Sanitizer Spray
81422-009-372022-07-29C16284748780-1e4f33bdf-abae-d8a0-e053-dadaa90a6e4e81422-009 Hand Sanitizer Spray
81422-009-502022-07-29C16284748780-1e4f33bdf-abae-d8a0-e053-dadaa90a6e4e81422-009 Hand Sanitizer Spray

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81422-009-00Hand Sanitizer500 mL in 1 BOTTLESPRAY5001
81422-009-37Hand Sanitizer3785 mL in 1 BOTTLESPRAY37851
81422-009-50Hand Sanitizer50 mL in 1 BOTTLESPRAY501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81422-009HAND SANITIZER (HAND SANITIZER SPRAY) SPRAY [SHENZHEN LYNNS INDUSTRIAL CO., LTD.]1Legacy NDC, 3 package rows20210119_b928aee4-bca5-7b8e-e053-2995a90a73c1.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81422-00981422-009-00, 81422-009-37, 81422-009-50

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
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
TROLAMINE9O3K93S3TKIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT

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
b928aee4-bca3-7b8e-e053-2995a90a73c1b928aee4-bca5-7b8e-e053-2995a90a73c12021-01-18WarningsExact identifier
spl id: b928aee4-bca3-7b8e-e053-2995a90a73c1
spl set id: b928aee4-bca5-7b8e-e053-2995a90a73c1

Reported adverse events (FAERS/openFDA)#

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