FDA.reportPublic FDA data

Rainbow Hand Sanitizer Blue

Manufacturer
Belleson Inc
Effective date
2021-10-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:42:35

Label at a glance#

ProductRainbow Hand Sanitizer Blue
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available. Warnings For external use only. Flammable. Keep away from heat or flame

Dosage and administration

• Place enough product on hands to cover all surfaces. Rub hands together until dry. • Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 68% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria that potentially can cause
disease. For use when soap and water are not available. Warnings
For external use only. Flammable. Keep away from heat or flame

Warnings

WARNINGS SECTION

Do not use
• in children less than 2 months of age
• on open skin wounds
When using this product keep out of eyes, ears, and mouth. In case
of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a
serious condition.

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

Directions

DOSAGE & ADMINISTRATION SECTION

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

SPL UNCLASSIFIED SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua, Glycerin, Aloe Vera Leaf, Mugwort Extract, Calendula Officinalis Flower,Camellia Sinensis Leaf Extract, Mulberry Root Extract, Licorice Extract,Rosmarinus Officinalis (Rosemary) Leaf Oil, Polysorbate 20, Fragrance,FD&C Blue No. 1

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1812262ethanol 68 % Topical SprayPSN1
1812262ethanol 0.68 ML/ML Topical SpraySCD1
1812262ethanol 68 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75063-0003-12022-07-29C16284748780-1e4f33bdf-aa7c-d8a0-e053-dadaa90a6e4e7f06bd31-4ee7-43ae-a76a-5dee613de466

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75063-0003-1Rainbow Hand Sanitizer Blue1 in 1 BOXLIQUID11
75063-0003-1Rainbow Hand Sanitizer Blue40 mL in 1 BOTTLE, SPRAYLIQUID401

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75063-0003RAINBOW HAND SANITIZER BLUE (ETHYL ALCOHOL) LIQUID [BELLESON INC]1Legacy NDC, 2 package rows20211003_7f06bd31-4ee7-43ae-a76a-5dee613de466.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75063-000375063-0003-1

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
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
ARTEMISIA PRINCEPS LEAFSY077EW02GIACT
CALENDULA OFFICINALIS FLOWERP0M7O4Y7YDIACT
MORUS ALBA ROOTCST1G9BZGDIACT
LICORICE61ZBX54883IACT
ROSEMARY OIL8LGU7VM393IACT
POLYSORBATE 207T1F30V5YHIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
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
cd4a9535-07b9-7da8-e053-2995a90a467e7f06bd31-4ee7-43ae-a76a-5dee613de4662021-10-01WarningsExact identifier
spl id: cd4a9535-07b9-7da8-e053-2995a90a467e
spl set id: 7f06bd31-4ee7-43ae-a76a-5dee613de466

Reported adverse events (FAERS/openFDA)#

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