FDA.reportPublic FDA data

HANNA Hand Sanitizer

Manufacturer
Rainbow Co Ltd
Effective date
2020-07-25
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:22:40

Label at a glance#

ProductHANNA Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

alcohol

INACTIVE INGREDIENT SECTION

WATER
DIPROPYLENE GLYCOL
CARBOMER
GLYCERIN
TRIETHANOLAMINE
PEG-60 HYDROGENATED CASTOR OIL
PANTHENOL
CAMELLIA SINENSIS LEAF EXTRACT
ALOE 8AR8ADENSIS LEAF EXTRACT
DIETHANOLAMINE
CITRUS PARADIS! (GRAPEFRUIT) PEEL OIL

OTC - PURPOSE SECTION

Sterilization of hands and skin

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

Apply to clean, dry hands. Apply sufficient amount to thoroughly wet all surfaces of hands and fingers. Rub onto hands until dry.

Supervise children in the use of this product.

WARNINGS SECTION

■ Flammable. Keep away from fire or flame.

■ For external use only.

■ Do not use in eyes.

■ lf swallowed, get medical help promptly.

■ Stop use, ask doctor lf irritation occurs.

■ Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN4
581662ethanol 0.7 ML/ML Topical GelSCD4
581662ethanol 70 % Topical GelSY4
581662ethyl alcohol 70 % Topical GelSY4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74247-0012-12021-07-23C16284748780-1c7ccaba7-1137-fd44-e053-dadaa90aa01bDrug Facts
74247-0012-22021-07-23C16284748780-1c7ccaba7-1137-fd44-e053-dadaa90aa01bDrug Facts
74247-0012-32021-07-23C16284748780-1c7ccaba7-1137-fd44-e053-dadaa90aa01bDrug Facts
74247-0012-42021-07-23C16284748780-1c7ccaba7-1137-fd44-e053-dadaa90aa01bDrug Facts
74247-0012-52021-07-23C16284748780-1c7ccaba7-1137-fd44-e053-dadaa90aa01bDrug Facts
74247-0012-62021-07-23C16284748780-1c7ccaba7-1137-fd44-e053-dadaa90aa01bDrug Facts
74247-0012-72021-07-23C16284748780-1c7ccaba7-1137-fd44-e053-dadaa90aa01bDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74247-0012-1HANNA Hand Sanitizer500 mL in 1 BOTTLEGEL5004
74247-0012-2HANNA Hand Sanitizer300 mL in 1 BOTTLEGEL3004
74247-0012-3HANNA Hand Sanitizer55 mL in 1 BOTTLEGEL554
74247-0012-4HANNA Hand Sanitizer100 mL in 1 BOTTLEGEL1004
74247-0012-5HANNA Hand Sanitizer2000 mL in 1 BOTTLEGEL20004
74247-0012-6HANNA Hand Sanitizer5000 mL in 1 BOTTLEGEL50004
74247-0012-7HANNA Hand Sanitizer3 mL in 1 POUCHGEL34

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74247-0012HANNA HAND SANITIZER (ALCOHOL) GEL [RAINBOW CO LTD]4Legacy NDC, 7 package rows20200726_a6995d91-3700-2686-e053-2995a90a2846.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74247-001274247-0012-1, 74247-0012-2, 74247-0012-3, 74247-0012-4, 74247-0012-5, 74247-0012-6, 74247-0012-7

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
GREEN TEA LEAFW2ZU1RY8B0IACT
GLYCERINPDC6A3C0OXIACT
GRAPEFRUIT PEEL3582N05Q44IACT
PEG-60 HYDROGENATED CASTOR OIL02NG325BQGIACT
DIETHANOLAMINEAZE05TDV2VIACT
PANTHENOLWV9CM0O67ZIACT
DIPROPYLENE GLYCOLE107L85C40IACT
ALOE VERA LEAFZY81Z83H0XIACT
CARBOMER 9404Q93RCW27EIACT
TROLAMINE9O3K93S3TKIACT
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
ab41892a-7629-35bf-e053-2a95a90a0945a6995d91-3700-2686-e053-2995a90a28462020-07-25WarningsExact identifier
spl id: ab41892a-7629-35bf-e053-2a95a90a0945
spl set id: a6995d91-3700-2686-e053-2995a90a2846

Reported adverse events (FAERS/openFDA)#

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