Nimbus 9 hand sanitizer 225ml

Manufacturer
Shenzhen Lantern Scicence Co Ltd | Lantern Beauty America,INC. | Shenzhen Lantern Science Co.,Ltd.
Effective date
2021-12-27
Label type
HUMAN OTC DRUG LABEL
Version
18
Source
full-release
Hydrated at
2026-05-31 23:46:11

Label at a glance#

ProductNimbus9 hand sanitizer 225ml 01
Active ingredientALCOHOL
Label structure10 sections

Dosage and administration

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

CH0012CH0012

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient Purpose

Ethyl Alcohol 71%(w/w) Antiseptic

USE

OTC - PURPOSE SECTION

Hand sanitizer to help reduce bacteria that potentially can cause disease.For use when soap and water are not available.

DOSAGE & ADMINISTRATION SECTION

Recommended for repeated use.

use anywhere without water.

Warning

WARNINGS SECTION

For external use only-hands.

Flammable,keep away from heat and 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.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water(Aqua),Glycerin,Propylene Glycol,Carbomer,Aminomethyl Propanol,Parfum.

Directions

INDICATIONS & USAGE SECTION

Place enough product on hands to cover all surfaces and rub hands together until dry.

Supervise children under 6 years of age when using this product to avoid swallowing.

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.

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.

Do not use

OTC - DO NOT USE SECTION

in children less than 2 months of age.

on open skin wounds and burns.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or rash occurs,these maybe signs of a serious condition.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CH0012 225MLCH0012 225ML

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1665370ethanol 71 % Topical SolutionPSN18
1665370ethanol 0.71 ML/ML Topical SolutionSCD18
1665370ethanol 71 % Topical SolutionSY18

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
54860-282-012023-01-30C16284748780-1f386c649-f562-0266-e053-dadaa90a7c1aLantern-Nimbus9 hand sanitizer 225mL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54860-282-01Nimbus9 hand sanitizer 225ml01191 g in 1 BOTTLE, PLASTICLIQUID19118

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54860-282NIMBUS9 HAND SANITIZER 225ML 01 (ALCOHOL) LIQUID [SHENZHEN LANTERN SCICENCE CO LTD]18Legacy NDC, 1 package rows20220101_a55cf302-48b2-1b93-e053-2995a90a78f9.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
54860-28254860-282-01

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 · 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
d46fbd88-ed31-7093-e053-2a95a90aa4c3a55cf302-48b2-1b93-e053-2995a90a78f92021-12-27WarningsExact identifier
spl id: d46fbd88-ed31-7093-e053-2a95a90aa4c3
spl set id: a55cf302-48b2-1b93-e053-2995a90a78f9

Reported adverse events (FAERS/openFDA)#

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