FDA.reportPublic FDA data

Heys Hand Sanitizer

Manufacturer
Heys America Ltd. | China Ningbo Shangge Cosmetic Technology Corp.
Effective date
2020-05-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:16:49

Label at a glance#

ProductHeys Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Storage and handling

Store at 20 C to 25 C (68 to 77 F) May discolor certain fabrics

Label contents#

Full prescribing information#

Heys Hand Sanitizer

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Heys Hand Sanitizer

OTC - PURPOSE SECTION

Antimicrobial

Heys Hand Sanitizer

INDICATIONS & USAGE SECTION

Use: Hand Sanitizer to help reduce bacteria on the skin.

Heys Hand Sanitizer

WARNINGS SECTION

Warnings: For external use only

Flammable: Keep away from heat and flame.

Heys Hand Sanitzer

OTC - WHEN USING SECTION

When using this product avoid contact with face, eyes, and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

Heys Hand Sanitizer

OTC - STOP USE SECTION

Stop use and ask a a doctor if irritation or redness develops.

Heys Hand Sanitizer

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Heys Hand Sanitizer

DOSAGE & ADMINISTRATION SECTION

Directions: wet hands thoroughly with product and rub into skin until dry. children under 6 years of age should be supervised by an adult when using.

Heys Hand Sanitizer

STORAGE AND HANDLING SECTION

Store at 20 C to 25 C (68 to 77 F)

May discolor certain fabrics

Heys Hand Sanitizer

INACTIVE INGREDIENT SECTION

Water

Carbomer 940

Fragrance

Glycerin

Polypropylene glycol

Triethanolamine

Aloe Barbadensis Leaf Juice

D-alpha Tocopheryl acetate

Heys Hand Sanitizer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

236 mL Label236 mL Label236 mL NDC: 77404-001-08

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77404-001-082022-07-29C16284748780-1e4f33bdf-a9fa-d8a0-e053-dadaa90a6e4eHeys Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77404-001-08Heys Hand Sanitizer236 mL in 1 BOTTLE, PLASTICGEL2361

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77404-001HEYS HAND SANITIZER (ETHYL ALCOHOL) GEL [HEYS AMERICA LTD.]1Legacy NDC, 1 package rows20200610_a4ecb2ea-9c64-2f08-e053-2995a90a04d8.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77404-00177404-001-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOMER 9404Q93RCW27EIACT
ALCOHOL3K9958V90MACTIB
TROLAMINE9O3K93S3TKIACT
.ALPHA.-TOCOPHEROL ACETATE, D-A7E6112E4NIACT
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT

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
a4ee7662-5b3e-26bf-e053-2995a90ad3d7a4ecb2ea-9c64-2f08-e053-2995a90a04d82020-05-05WarningsExact identifier
spl id: a4ee7662-5b3e-26bf-e053-2995a90ad3d7
spl set id: a4ecb2ea-9c64-2f08-e053-2995a90a04d8

Reported adverse events (FAERS/openFDA)#

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