Mellow hand sanitizer 236ml ML312

Manufacturer
Shenzhen Lantern Science Co.,Ltd | Lantern Beauty America,INC. | Shenzhen Lantern Science Co., Ltd.
Effective date
2020-05-04
Label type
HUMAN OTC DRUG LABEL
Version
14
Source
full-release
Hydrated at
2026-05-31 23:09:35

Label at a glance#

ProductMellow hand sanitizer 236ml ML312 01
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

wet hands thoroughyly with product and rub until dry without wiping. For children under 6,use only under adult supervision. Not recommended for infants. 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

ML 312 label artwork 8ozML 312 label artwork 8oz

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients Purpose

Ethyl Alcohol 62% Antiseptic

Feature

OTC - PURPOSE SECTION

To decrease bacteria on the skin that could cause disease.

Recommended for repeated use.

Use anywhere without water.

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.

Inactive ingredients

INACTIVE INGREDIENT SECTION

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.

For children under 6,use only under adult supervision.

Not recommended for infants.

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.

OTHER SAFETY INFORMATION

Do not store above100℉(38℃)

May discolor some fabrics.

Harmful to wood finishes and plastics.

When using this product

OTC - WHEN USING SECTION

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

Do not inhale or ingest.

Avoid contact with broken skin.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ML 312 label artworkML 312 label artwork

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN14
581660ethanol 0.62 ML/ML Topical GelSCD14
581660ethanol 62 % Topical GelSY14

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
54860-244-012022-01-28C16284748780-1d6a99b39-704e-a426-e053-dadaa90af4c2Mellow hand sanitizer 236ml ML312

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54860-244-01Mellow hand sanitizer 236ml ML31201236 mL in 1 BOTTLE, PLASTICLIQUID23614

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54860-244MELLOW HAND SANITIZER 236ML ML312 01 (ALCOHOL) LIQUID [SHENZHEN LANTERN SCIENCE CO.,LTD]14Legacy NDC, 1 package rows20200505_a4ced26d-27db-33d2-e053-2995a90a8252.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
54860-24454860-244-01

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

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
a4ceaeea-934d-6a86-e053-2995a90a3c08a4ced26d-27db-33d2-e053-2995a90a82522020-05-04WarningsExact identifier
spl id: a4ceaeea-934d-6a86-e053-2995a90a3c08
spl set id: a4ced26d-27db-33d2-e053-2995a90a8252

Reported adverse events (FAERS/openFDA)#

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