KEKE hand sanitizer 59ml keke59

Manufacturer
Shenzhen Lantern Science Co.,Ltd | Lantern Beauty America,INC. | Shenzhen Lantern Science Co., Ltd.
Effective date
2020-06-09
Label type
HUMAN OTC DRUG LABEL
Version
11
Source
full-release
Hydrated at
2026-05-31 23:16:49

Label at a glance#

ProductInstant hand sanitizer 01
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

wet hands thoroughyly with product and rub until dry without wiping. 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

instant hand sanitizerinstant hand sanitizer

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients Purpose

Ethyl Alcoh75% (v/v) Antiseptic

Features

OTC - PURPOSE SECTION

To decrease bacteria on the skin that could cause disease.

Recommended for repeated use.

Use anywhere without water.

purpose

OTC - PURPOSE SECTION

ANTISEPTIC

DOSAGE & ADMINISTRATION SECTION

Recommended for repeated use.

use anywhere without water.

Warning

WARNINGS SECTION

For external use only:hands,avoid ayes ,in case of eye contact, flush with water.

flammable,keep away from heat and flame.

Discontinue if skin becomes irritated and ask a doctor.

keep out of reach of children,in case of accidenal ingestion.seek professional assistance or contact a poison control center immediately.

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.

Non-Medicinal

INACTIVE INGREDIENT SECTION

Aqua(water),Isopropyl Alcohol,Glycerin,Carbomer,Aminomethyl Propanol,Parfum,Propylene Glycol,ISOPROPYL MYRISTATE,ALOE BARBADENSIS LEAF JUICE,Tocopheryl Acetate,FD&C Yellow No.5(Tartrazine),FD&C Blue No.1.

Directions

INDICATIONS & USAGE SECTION

wet hands thoroughyly with product and rub until dry without wiping.

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

instant hand sanitizer.jpginstant hand sanitizer.jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1047755ethanol 75 % Topical SolutionPSN11
1047755ethanol 0.75 ML/ML Topical SolutionSCD11
1047755ethanol 75 % Topical SolutionSY11

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
54860-287-012022-01-28C16284748780-1d6a99b39-a8c3-a426-e053-dadaa90af4c2instant hand sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54860-287-01Instant hand sanitizer0159 mL in 1 BOTTLELIQUID5911

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54860-287INSTANT HAND SANITIZER 01 (ALCOHOL) LIQUID [SHENZHEN LANTERN SCIENCE CO.,LTD]11Legacy NDC, 1 package rows20200610_a42927e9-c0a9-3089-e053-2995a90aaf69.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
54860-28754860-287-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Source Document#

Source XML · Source PDF

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
a7a073ff-cc3f-a5e0-e053-2995a90a4f84a42927e9-c0a9-3089-e053-2995a90aaf692020-06-09WarningsExact identifier
spl id: a7a073ff-cc3f-a5e0-e053-2995a90a4f84
spl set id: a42927e9-c0a9-3089-e053-2995a90aaf69

Reported adverse events (FAERS/openFDA)#

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