FDA.reportPublic FDA data

Divine Tree Hand Sanitizer Gel

Manufacturer
K.BIOCOS
Effective date
2020-06-04
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:16:15

Label at a glance#

ProductDivine Tree Hand Sanitizer Gel
Active ingredientALCOHOL
Label structure13 sections

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.

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v. Purpose Antiseptic

Active IngredientActive Ingredient

Purpose(s)

OTC - PURPOSE SECTION

Purpose-Antiseptic

Purpose(s)Purpose(s)

Use(s)

INDICATIONS & USAGE SECTION

Health care personnel hand rub to help reduce bacteria that potentially can cause disease.

Use(s)Use(s)

Warnings

WARNINGS SECTION

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

WarningsWarnings

Do not use

OTC - DO NOT USE SECTION

  • In children less than 2 months of age
  • on open skin wounds

Do not useDo not use

When Using This Product

OTC - WHEN USING SECTION

When Using This Product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

When Using This ProductWhen Using This Product

Stop Use and Ask a Doctor

OTC - STOP USE SECTION

Stop Use and Ask a Doctor if irritation or rash occurs. These may be signs of a serious condition.

Stop Use and Ask a DoctorStop Use and Ask a Doctor

Keep Out Of Reach Of Children

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.

Keep Out Of Reach Of ChildrenKeep Out Of Reach Of Children

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.

DirectionsDirections

Other Information

STORAGE AND HANDLING SECTION

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

Other InformationOther Information

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients-Water, Glycerin, Carbomer, Aminomethyl Propanol, Mentha Arvensis Leaf Oil, Tocopheryl Acetate, Panthenol, Sodium Hyaluronate, Aloe Barbadensis Leaf Extract

Inactive IngredientsInactive Ingredients

Questions Or Comments

OTC - QUESTIONS SECTION

Questions Or Comments-1-800-819-4159

Questions Or CommentsQuestions Or Comments

Pakage Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Divine Tree
Hand Sanitizer Gel
Non-Sterile Solution
Help Reduce Bacteria on the skin

  • For All Day Use
  • No Sticky
  • Deep Moisturizing

500ml 16.9 fl.oz

Pakage LabelPakage Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN4
582753ethanol 0.7 ML/ML Topical SolutionSCD4
582753ethanol 70 % Topical SolutionSY4
582753ethyl alcohol 70 % Topical SolutionSY4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73494-500-022022-01-28C16284748780-1d6a99b39-c1bf-a426-e053-dadaa90af4c2Divine Tree Hand Sanitizer Gel 500ml

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73494-500-01Divine Tree Hand Sanitizer Gel500 mL in 1 BOTTLELIQUID5004
73494-500-02Divine Tree Hand Sanitizer Gel24 in 1 CASELIQUID244

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73494-500DIVINE TREE HAND SANITIZER GEL (ETHYL ALCOLHOL) LIQUID [K.BIOCOS]4Legacy NDC, 2 package rows20200606_a2843fb1-cc8f-1119-e053-2995a90a6699.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73494-50073494-500-01, 73494-500-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
MENTHA ARVENSIS LEAF OIL1AEY1M553NIACT
HYALURONATE SODIUMYSE9PPT4THIACT
PANTHENOLWV9CM0O67ZIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER 9404Q93RCW27EIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
.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
a74ce3f0-9ed7-1c24-e053-2995a90a4ec8a2843fb1-cc8f-1119-e053-2995a90a66992020-06-04WarningsExact identifier
spl id: a74ce3f0-9ed7-1c24-e053-2995a90a4ec8
spl set id: a2843fb1-cc8f-1119-e053-2995a90a6699

Reported adverse events (FAERS/openFDA)#

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