Mellow hand sanitizer 59ml

Manufacturer
Shenzhen Lantern Science Co.,Ltd. | Lantern Beauty America,INC. | Shenzhen Lantern Science Co., Ltd.
Effective date
2020-09-02
Label type
HUMAN OTC DRUG LABEL
Version
21
Source
full-release
Hydrated at
2026-05-31 23:26:48

Label at a glance#

ProductMellow hand sanitizer 59ml 01
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Dosage and administration

Take a palmful(5 grams) of product in one hand. Spread on both hands and rub into skin. 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

Mellow hand sanitizer 59mlMellow hand sanitizer 59ml

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients Purpose

Benzalkonium Chloride 0.1% Antiseptic

Warning

WARNINGS SECTION

For external use only.

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

Aqua,Hydroxyethylcollulose,Phenoxyethanol,Polysorbate 20,Disodium EDTA,Parfum.

Directions

INDICATIONS & USAGE SECTION

Take a palmful(5 grams) of product in one hand.

Spread on both hands and rub into skin.

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.

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes,if contact occurs,rinse eyes thoroughly with water.

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.

Stop use and ask a doctor

OTC - STOP USE SECTION

stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.

Use

OTC - PURPOSE SECTION

For handwashing to decrease bacteria on the skin.

OTHER SAFETY INFORMATION

Do not store above105℉

May discolor some fabrics

Harmful to wood finishes and plastics.

dosage

DOSAGE & ADMINISTRATION SECTION

take a palmful(5 grams) of product in one hand.

spread on both hands and rub into skin.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Mellow hand sanitizer 59mlMellow hand sanitizer 59ml

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038791benzalkonium chloride 0.1 % Topical SolutionPSN21
1038791benzalkonium chloride 1 MG/ML Topical SolutionSCD21
1038791benzalkonium chloride 0.1 % Topical SolutionSY21

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
54860-329-012022-01-28C16284748780-1d6a99b39-7b5d-a426-e053-dadaa90af4c2Mellow hand sanitizer 59ml

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54860-329-01Mellow hand sanitizer 59ml0159 mL in 1 BOTTLE, PLASTICLIQUID5921

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54860-329MELLOW HAND SANITIZER 59ML 01 (BENZALKONIUM CHLORIDE) LIQUID [SHENZHEN LANTERN SCIENCE CO.,LTD.]21Legacy NDC, 1 package rows20200904_ae5f8a72-1510-1429-e053-2995a90a46e2.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54860-32954860-329-01

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
ae5f9d87-d1a0-51cd-e053-2a95a90a7d24ae5f8a72-1510-1429-e053-2995a90a46e22020-09-02WarningsExact identifier
spl id: ae5f9d87-d1a0-51cd-e053-2a95a90a7d24
spl set id: ae5f8a72-1510-1429-e053-2995a90a46e2

Reported adverse events (FAERS/openFDA)#

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