ANTIBACTERIAL HAND GEL Dippin Dots Banana Split

Manufacturer
JFL ENTERPRISES, INC | NingBo Huize Commodity Co.,Ltd.
Effective date
2018-01-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:54:48

Label at a glance#

ProductHand Sanitizer Banana Split
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Rub hands thoroughly with product and allow to dry.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Decrease bacteria on hands

Warnings

WARNINGS SECTION

External Use Only. DO NOT EAT.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

if swallowed get medical help or contact a Poison Control Center right away.

WARNINGS SECTION

Flammable: Keep away from flame or high heat

Directions

DOSAGE & ADMINISTRATION SECTION

Rub hands thoroughly with product and allow to dry.

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Carbomer, Glycerin, Jojoba Particles, Banana & Chocolate Extract, Pigment Yellow GB34-2030, Yellow 109C, Propylene Glycol, Triethanolamine, Water.

Stop and Ask a doctor if

OTC - STOP USE SECTION

Irritation or redness develop.

HAND SANITIZER (ALCOHOL) GEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label Image
Label Image

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN1
581660ethanol 0.62 ML/ML Topical GelSCD1
581660ethanol 62 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71246-4012-1Hand Sanitizer Banana Split40 mL in 1 POUCHGEL401

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71246-4012HAND SANITIZER BANANA SPLIT (ALCOHOL) GEL [JFL ENTERPRISES, INC]1Legacy NDC, 1 package rows20180301_e0dccfde-b49d-4a02-8962-748ab35feffc.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
71246-401271246-4012-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

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
f20c7ee7-cb2e-40b8-8704-182ec3f60696e0dccfde-b49d-4a02-8962-748ab35feffc2018-01-01WarningsExact identifier
spl id: f20c7ee7-cb2e-40b8-8704-182ec3f60696
spl set id: e0dccfde-b49d-4a02-8962-748ab35feffc

Reported adverse events (FAERS/openFDA)#

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