KEKE hand sanitizer 750ml

Manufacturer
Shenzhen Lantern Scicence Co.,Ltd. | LANTERN HEALTH&BEAUTY LAB INC. | Shenzhen Lantern Science Co.,Ltd.
Effective date
2021-02-28
Label type
HUMAN OTC DRUG LABEL
Version
21
Source
full-release
Hydrated at
2026-05-31 23:38:38

Label at a glance#

ProductKEKE hand sanitizer 750ml 01
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

place enough product in your palm rub hands vigorously until dry children under 6 years of age should be supervised when using this product. When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water. Do not inhale or ingest. Avoid contact with broken skin. Do not store above 105F. May discolor some fabrics. Harmful to wood finishes and plastics.

Label contents#

Full prescribing information#

Drug Facts

DESCRIPTION SECTION

KEKE hand sanitizer 750mlKEKE hand sanitizer 750ml

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient Purpose

Ethyl Alcohol 75%(V/V) Antiseptic

Use

OTC - PURPOSE SECTION

Hand sanitizer helps to reduce bacteria that potentially can cause disease.

Warning

WARNINGS SECTION

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

WARNINGS AND PRECAUTIONS SECTION

For external use only.

Flammable, keep away from heat and flame.

OTC - STOP USE SECTION

Discontinue if skin becomes irritated and ask a doctor .

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a poson control center immediately.

When using this product

OTC - WHEN USING SECTION

do not get into eyes,If contact occurs,rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

If iritation or rash appears and lasts.

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.

DOSAGE & ADMINISTRATION SECTION

Recommended for repeated use.

use anywhere without water.

Directions

INDICATIONS & USAGE SECTION

place enough product in your palm

rub hands vigorously until dry

children under 6 years of age should be supervised when using this product.

OTC - DO NOT USE SECTION

When using this product

keep out of eyes. In case of contact with eyes, flush thoroughly with water.

Do not inhale or ingest.

Avoid contact with broken skin.

Other information

CLEANING, DISINFECTING, AND STERILIZATION INSTRUCTIONS

Do not store above 105F.

May discolor some fabrics.

Harmful to wood finishes and plastics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water(Aqua),Glycerin,Propylene Glycol,,Carbomer,Aminomethyl propanolFragrance,

Other information

OTHER SAFETY INFORMATION

Store between 106℉(41℃).

May discolor certain fabrics or surfaces.

Purpose

OTC - PURPOSE SECTION

Antiseptic

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

keke hand sanitizer 750mlkeke hand sanitizer 750ml

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1047755ethanol 75 % Topical SolutionPSN21
1047755ethanol 0.75 ML/ML Topical SolutionSCD21
1047755ethanol 75 % Topical SolutionSY21

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
54860-372-012023-01-30C16284748780-1f386c64a-469e-0266-e053-dadaa90a7c1aKEKE hand sanitizer 750ml

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54860-372-01KEKE hand sanitizer 750ml01750 mL in 1 BOTTLE, PLASTICLIQUID75021

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54860-372KEKE HAND SANITIZER 750ML 01 (ALCOHOL) LIQUID [SHENZHEN LANTERN SCICENCE CO.,LTD.]21Legacy NDC, 1 package rows20210301_abf36d3c-9e69-6616-e053-2a95a90a43fa.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54860-37254860-372-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
bc719bc8-265f-08e1-e053-2a95a90a246eabf36d3c-9e69-6616-e053-2a95a90a43fa2021-02-28WarningsExact identifier
spl id: bc719bc8-265f-08e1-e053-2a95a90a246e
spl set id: abf36d3c-9e69-6616-e053-2a95a90a43fa

Reported adverse events (FAERS/openFDA)#

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